LEP, leptin, 3952

N. diseases: 931; N. variants: 15
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894023
rs104894023
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C3554224
Disease:
LEPTIN DEFICIENCY OR DYSFUNCTION
0.800 GeneticVariation UNIPROT A leptin missense mutation associated with hypogonadism and morbid obesity. 9500540 1998
dbSNP: rs104894023
rs104894023
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C3554224
Disease:
LEPTIN DEFICIENCY OR DYSFUNCTION
T 0.800 CausalMutation CLINVAR
dbSNP: rs104894023
rs104894023
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C3554224
Disease:
LEPTIN DEFICIENCY OR DYSFUNCTION
0.800 GeneticVariation UNIPROT Biologically inactive leptin and early-onset extreme obesity. 25551525 2015
dbSNP: rs13228377
rs13228377
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0004096
Disease:
Asthma
0.010 GeneticVariation BEFREE We observed that LEP polymorphism (rs13228377) was associated with higher serum leptin levels in asthma and these two variables had high predictive value for asthma risk (P = 0.007, odds ratio 17.5, predictive accuracy 83.9%). 30203371 2018
dbSNP: rs1554394014
rs1554394014
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C3554224
Disease:
LEPTIN DEFICIENCY OR DYSFUNCTION
C 0.700 GeneticVariation CLINVAR
dbSNP: rs1800564
rs1800564
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0001973
Disease:
Alcoholic Intoxication, Chronic
0.010 GeneticVariation BEFREE In this study, we explored whether functionally relevant genetic polymorphisms in SRD5A2 (V89L, A49T, [TA](n)) are linked to alcohol addiction and craving. 22707254 2012
dbSNP: rs199647957
rs199647957
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE The IL-6 G174C polymorphism was also associated obesity when using allelic comparisons, the recessive genetic model and the dominant genetic model with OR (95% CI) of 1.95 (1.37-2.77), 1.44 (1.15-1.80), and 1.36 (1.16-1.59), respectively. 21660081 2012
dbSNP: rs200343690
rs200343690
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE This study was to investigate the prevalence of single nucleotide polymorphisms (SNPs) in RETN gene 420C/G; 44G/A; 62G/A; 394C/G and 299 G/A and their association with Resistin level and obesity in Tunisian volunteers. 28393393 2018
dbSNP: rs200487063
rs200487063
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.010 GeneticVariation BEFREE Near the sites binding to TATA-binding protein (TBP) in human gene promoters, we found 22 obesity-related candidate SNP markers, including rs10895068 (male breast cancer in obesity); rs35036378 (reduced risk of obesity after ovariectomy); rs201739205 (reduced risk of obesity-related cancers due to weight loss by diet/exercise in obese postmenopausal women); rs183433761 (obesity resistance during a high-fat diet); rs367732974 and rs549591993 (both: cardiovascular complications in obese patients with type 2 diabetes mellitus); rs200487063 and rs34104384 (both: obesity-caused hypertension); rs35518301, rs72661131, and rs562962093 (all: obesity); and rs397509430, rs33980857, rs34598529, rs33931746, rs33981098, rs34500389, rs63750953, rs281864525, rs35518301, and rs34166473 (all: chronic inflammation in comorbidities of obesity). 26694100 2015
dbSNP: rs200487063
rs200487063
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0242787
Disease:
Malignant neoplasm of male breast
0.010 GeneticVariation BEFREE Near the sites binding to TATA-binding protein (TBP) in human gene promoters, we found 22 obesity-related candidate SNP markers, including rs10895068 (male breast cancer in obesity); rs35036378 (reduced risk of obesity after ovariectomy); rs201739205 (reduced risk of obesity-related cancers due to weight loss by diet/exercise in obese postmenopausal women); rs183433761 (obesity resistance during a high-fat diet); rs367732974 and rs549591993 (both: cardiovascular complications in obese patients with type 2 diabetes mellitus); rs200487063 and rs34104384 (both: obesity-caused hypertension); rs35518301, rs72661131, and rs562962093 (all: obesity); and rs397509430, rs33980857, rs34598529, rs33931746, rs33981098, rs34500389, rs63750953, rs281864525, rs35518301, and rs34166473 (all: chronic inflammation in comorbidities of obesity). 26694100 2015
dbSNP: rs200487063
rs200487063
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE Near the sites binding to TATA-binding protein (TBP) in human gene promoters, we found 22 obesity-related candidate SNP markers, including rs10895068 (male breast cancer in obesity); rs35036378 (reduced risk of obesity after ovariectomy); rs201739205 (reduced risk of obesity-related cancers due to weight loss by diet/exercise in obese postmenopausal women); rs183433761 (obesity resistance during a high-fat diet); rs367732974 and rs549591993 (both: cardiovascular complications in obese patients with type 2 diabetes mellitus); rs200487063 and rs34104384 (both: obesity-caused hypertension); rs35518301, rs72661131, and rs562962093 (all: obesity); and rs397509430, rs33980857, rs34598529, rs33931746, rs33981098, rs34500389, rs63750953, rs281864525, rs35518301, and rs34166473 (all: chronic inflammation in comorbidities of obesity). 26694100 2015
dbSNP: rs200487063
rs200487063
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE Near the sites binding to TATA-binding protein (TBP) in human gene promoters, we found 22 obesity-related candidate SNP markers, including rs10895068 (male breast cancer in obesity); rs35036378 (reduced risk of obesity after ovariectomy); rs201739205 (reduced risk of obesity-related cancers due to weight loss by diet/exercise in obese postmenopausal women); rs183433761 (obesity resistance during a high-fat diet); rs367732974 and rs549591993 (both: cardiovascular complications in obese patients with type 2 diabetes mellitus); rs200487063 and rs34104384 (both: obesity-caused hypertension); rs35518301, rs72661131, and rs562962093 (all: obesity); and rs397509430, rs33980857, rs34598529, rs33931746, rs33981098, rs34500389, rs63750953, rs281864525, rs35518301, and rs34166473 (all: chronic inflammation in comorbidities of obesity). 26694100 2015
dbSNP: rs200487063
rs200487063
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0238033
Disease:
Carcinoma of Male Breast
0.010 GeneticVariation BEFREE Near the sites binding to TATA-binding protein (TBP) in human gene promoters, we found 22 obesity-related candidate SNP markers, including rs10895068 (male breast cancer in obesity); rs35036378 (reduced risk of obesity after ovariectomy); rs201739205 (reduced risk of obesity-related cancers due to weight loss by diet/exercise in obese postmenopausal women); rs183433761 (obesity resistance during a high-fat diet); rs367732974 and rs549591993 (both: cardiovascular complications in obese patients with type 2 diabetes mellitus); rs200487063 and rs34104384 (both: obesity-caused hypertension); rs35518301, rs72661131, and rs562962093 (all: obesity); and rs397509430, rs33980857, rs34598529, rs33931746, rs33981098, rs34500389, rs63750953, rs281864525, rs35518301, and rs34166473 (all: chronic inflammation in comorbidities of obesity). 26694100 2015
dbSNP: rs2071045
rs2071045
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0031046
Disease:
Pericarditis
0.010 GeneticVariation BEFREE However, further analysis in patients with SLE showed that the TT genotype and T allele frequencies of the LEP rs2071045 polymorphism were nominally significantly higher in patients with pericarditis (P = 0.012, P = 0.011, respectively). 28244652 2017
dbSNP: rs2071045
rs2071045
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0027794
Disease:
Neural Tube Defects
0.010 GeneticVariation BEFREE Additionally, maternal LEP rs2071045 (RR = 1.31, 95% CI: 1.08, 1.60) and offspring UCP2 rs660339 (RR = 1.32, 95% CI: 1.06, 1.64) were associated with NTD risk. 23132673 2012
dbSNP: rs2071045
rs2071045
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0024141
Disease:
Lupus Erythematosus, Systemic
0.010 GeneticVariation BEFREE However, further analysis in patients with SLE showed that the TT genotype and T allele frequencies of the LEP rs2071045 polymorphism were nominally significantly higher in patients with pericarditis (P = 0.012, P = 0.011, respectively). 28244652 2017
dbSNP: rs2167270
rs2167270
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0009402
Disease:
Colorectal Carcinoma
0.020 GeneticVariation BEFREE Two variants in the leptin gene showed statistically significant associations with CRC among women: LEP rs2167270 (OR = 1.13, 95% CI: 1.06-1.21) and LEP rs4731426 (OR = 1.09, 95% CI: 1.02-1.17). 30379922 2018
dbSNP: rs2167270
rs2167270
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C1306459
Disease:
Primary malignant neoplasm
0.020 GeneticVariation BEFREE Leptin rs2167270 G > A (G19A) polymorphism may decrease the risk of cancer: A case-control study and meta-analysis involving 19 989 subjects. 30697798 2019
dbSNP: rs2167270
rs2167270
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0006826
Disease:
Malignant Neoplasms
0.020 GeneticVariation BEFREE Leptin rs2167270 G > A (G19A) polymorphism may decrease the risk of cancer: A case-control study and meta-analysis involving 19 989 subjects. 30697798 2019
dbSNP: rs2167270
rs2167270
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0009402
Disease:
Colorectal Carcinoma
0.020 GeneticVariation BEFREE These findings suggest that the LEP A19G (rs2167270) genetic polymorphism may decrease the susceptibility to cancers in colorectal cancer and non-Hodgkin's lymphoma, when assuming a homozygote codominant model and a recessive genetic model among Latin American population. 24845032 2014
dbSNP: rs2167270
rs2167270
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C1306459
Disease:
Primary malignant neoplasm
0.020 GeneticVariation BEFREE Overall, the LEP A19G (rs2167270) genetic polymorphism was associated with lower cancer risk. 24845032 2014
dbSNP: rs2167270
rs2167270
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0006826
Disease:
Malignant Neoplasms
0.020 GeneticVariation BEFREE Overall, the LEP A19G (rs2167270) genetic polymorphism was associated with lower cancer risk. 24845032 2014
dbSNP: rs2167270
rs2167270
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0007222
Disease:
Cardiovascular Diseases
0.010 GeneticVariation BEFREE LEP rs2167270 polymorphism does not seem to be a genetic risk factor for disease susceptibility or clinically evident CV disease and subclinical atherosclerosis in patients with RA. 21385539 2011
dbSNP: rs2167270
rs2167270
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C0699790
Disease:
Colon Carcinoma
0.010 GeneticVariation BEFREE We observed a slight reduction in colon cancer risk with the AA LEP rs2167270 genotype (OR 0.79 95% CI 0.64, 0.98) and although not reaching statistical significance, with the combined GG LEP rs2167270 and GG LEPR rs6588147 (OR 0.70, 95% CI 0.49, 1.02) genotypes. 18059035 2008
dbSNP: rs2167270
rs2167270
Entrez Id: 3952
Gene Symbol: LEP
LEP
CUI: C2239176
Disease:
Liver carcinoma
0.010 GeneticVariation BEFREE This case-control study highlights that <i>LEP</i> rs7799039 A>G and rs2167270 G>A polymorphisms increase the susceptibility to HCC; however, <i>LEPR</i> rs6588147 G>A polymorphism may be a protective factor for HCC in Eastern Chinese Han population. 29695916 2018