GHRL, ghrelin and obestatin prepropeptide, 51738

N. diseases: 183; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4684677
rs4684677
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0028754
Disease:
Obesity
0.710 GeneticVariation BEFREE Replication of the nominal associations with obesity could not be confirmed in a German genome-wide association (GWA) study for rs4684677 and rs572169 polymorphisms. 19165163 2009
dbSNP: rs34911341
rs34911341
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0028754
Disease:
Obesity
0.710 GeneticVariation BEFREE Arg51Gln mutation was associated with lower plasma ghrelin levels but not with obesity. 12181387 2002
dbSNP: rs34911341
rs34911341
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0028754
Disease:
Obesity
T 0.710 SusceptibilityMutation CLINVAR
dbSNP: rs4684677
rs4684677
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0028754
Disease:
Obesity
A 0.710 SusceptibilityMutation CLINVAR
dbSNP: rs3732950
rs3732950
Entrez Id: 6396;51738;100126793
Gene Symbol: SEC13;GHRL;GHRLOS
SEC13;GHRL;GHRLOS
CUI: C0202236
Disease:
Triglycerides measurement
0.700 GeneticVariation GWASDB Large-scale gene-centric meta-analysis across 32 studies identifies multiple lipid loci. 23063622 2012
dbSNP: rs34911341
rs34911341
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C2676079
Disease:
METABOLIC SYNDROME, SUSCEPTIBILITY TO
T 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C2676079
Disease:
METABOLIC SYNDROME, SUSCEPTIBILITY TO
T 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C4016925
Disease:
OBESITY, AGE AT ONSET OF
T 0.700 CausalMutation CLINVAR
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.060 GeneticVariation BEFREE MTLRP genetic polymorphism (214C>A) was associated with Type 2 diabetes in Caucasian population: a meta-analysis. 25095788 2014
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.060 GeneticVariation BEFREE The GHRL Leu72Met polymorphism may help to maintain normal renal function and may protect against the development of DN by reducing albuminuria and improving renal function in Chinese patients with type 2 diabetes. 24132517 2014
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.060 GeneticVariation BEFREE The Leu72Met polymorphism of the preproghrelin gene was not associated with T2DM in Chinese population. 22441120 2012
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.060 GeneticVariation BEFREE Recent studies have shown that the preproghrelin Leu72Met polymorphism is associated with serum creatinine (Scr) concentration in type 2 diabetes; 72Met carriers exhibited lower Scr levels as compared with the 72Met non-carriers. 16793966 2006
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.060 GeneticVariation BEFREE Our data indicate that the preproghrelin Leu72Met polymorphism is not associated with type 2 diabetes mellitus. 16483881 2006
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent
0.060 GeneticVariation BEFREE The Leu72Met polymorphism of the preproghrelin gene was not related to cardiovascular disease in type 2 diabetes mellitus patients. 12974878 2003
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0028754
Disease:
Obesity
0.050 GeneticVariation BEFREE Average dietary energy in lunch, rs3782886, and rs696217 were associated with obesity, and rs3782886 was associated with other metabolic abnormalities. 27245511 2019
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0028754
Disease:
Obesity
0.050 GeneticVariation BEFREE Minor homozygotes for five preproghrelin gene polymorphisms, namely, -1500C>G (rs3755777), -1062G>C (rs26311), -994C>T (rs26312) (promoter region), Leu72Met (rs696217) (exon 2), and +3056T>C (rs2075356) (intron 2), had high values of total and visceral fat areas, waist circumference, and BMI, indicating significant correlation of the polymorphisms with obesity and fat metabolism. 23257630 2013
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0028754
Disease:
Obesity
0.050 GeneticVariation BEFREE The Leu72Met (+408C>A) polymorphism of the preproghrelin, has been linked to obesity, insulin resistance and diabetes. 22441120 2012
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0028754
Disease:
Obesity
0.050 GeneticVariation BEFREE The Leu72Met (+408C>A) polymorphic variant of the preproghrelin, the gene for the ghrelin precursor, has been linked to obesity, diabetes and metabolic syndrome. 17884032 2008
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0028754
Disease:
Obesity
0.050 GeneticVariation BEFREE The frequencies of the Leu72Met polymorphism were 29.3% in obese, 32.3% in overweight, and 32.5% in lean Korean children. 16459454 2005
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0011881
Disease:
Diabetic Nephropathy
0.020 GeneticVariation BEFREE The GHRL Leu72Met polymorphism may help to maintain normal renal function and may protect against the development of DN by reducing albuminuria and improving renal function in Chinese patients with type 2 diabetes. 24132517 2014
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0011847
Disease:
Diabetes
0.020 GeneticVariation BEFREE The Leu72Met (+408C>A) polymorphism of the preproghrelin, has been linked to obesity, insulin resistance and diabetes. 22441120 2012
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0011849
Disease:
Diabetes Mellitus
0.020 GeneticVariation BEFREE The Leu72Met (+408C>A) polymorphism of the preproghrelin, has been linked to obesity, insulin resistance and diabetes. 22441120 2012
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0524620
Disease:
Metabolic Syndrome X
0.020 GeneticVariation BEFREE The Leu72Met (+408C>A) polymorphic variant of the preproghrelin, the gene for the ghrelin precursor, has been linked to obesity, diabetes and metabolic syndrome. 17884032 2008
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0020538
Disease:
Hypertensive disease
0.020 GeneticVariation BEFREE The Leu72Met polymorphism was not associated with hypertension, diabetes, dyslipidemia, the number of diseased vessels, plasma total cholesterol, triglyceride, high density lipoprotein cholesterol, low density lipoprotein cholesterol or fasting glucose levels in CAD patients. 17884032 2008
dbSNP: rs696217
rs696217
Entrez Id: 51738;100126793
Gene Symbol: GHRL;GHRLOS
GHRL;GHRLOS
CUI: C0011849
Disease:
Diabetes Mellitus
0.020 GeneticVariation BEFREE The frequency of the Leu72Met polymorphism in diabetic nephropathy was significantly lower in patients with renal dysfunction (15.9%, P < 0.01) than in patients with normal renal function (42.0%) or in the diabetes control group (40.6%). 16793966 2006