CCK, cholecystokinin, 885

N. diseases: 326; N. variants: 7
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs754635
rs754635
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Genetic analyses of diverse populations improves discovery for complex traits. 31217584 2019
dbSNP: rs10460960
rs10460960
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C1305855
Disease:
Body mass index 		G 0.700 GeneticVariation GWASCAT A Large Multiethnic Genome-Wide Association Study of Adult Body Mass Index Identifies Novel Loci. 30108127 2018
dbSNP: rs10460960
rs10460960
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 112 new loci for body mass index in the Japanese population. 28892062 2017
dbSNP: rs754635
rs754635
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C4049938
Disease:
Physical Activity Measurement 		G 0.700 GeneticVariation GWASCAT Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. 28448500 2017
dbSNP: rs754635
rs754635
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C1305855
Disease:
Body mass index 		G 0.700 GeneticVariation GWASCAT Genome-wide physical activity interactions in adiposity - A meta-analysis of 200,452 adults. 28448500 2017
dbSNP: rs8192473
rs8192473
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C1305855
Disease:
Body mass index 		T 0.700 GeneticVariation GWASCAT Genome-wide association study identifies 112 new loci for body mass index in the Japanese population. 28892062 2017
dbSNP: rs8192472
rs8192472
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children. 24348519 2013
dbSNP: rs8192472
rs8192472
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C0005893
Disease:
Body mass index procedure 		A 0.700 GeneticVariation GWASDB EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children. 24348519 2013
dbSNP: rs8192472
rs8192472
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C0578022
Disease:
Finding of body mass index 		A 0.700 GeneticVariation GWASDB EMR-linked GWAS study: investigation of variation landscape of loci for body mass index in children. 24348519 2013
dbSNP: rs4377469
rs4377469
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C1305855
Disease:
Body mass index 		T 0.700 GeneticVariation GWASCAT Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations. 22344221 2012
dbSNP: rs4377469
rs4377469
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C0578022
Disease:
Finding of body mass index 		T 0.700 GeneticVariation GWASDB Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations. 22344221 2012
dbSNP: rs4377469
rs4377469
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C0005893
Disease:
Body mass index procedure 		T 0.700 GeneticVariation GWASDB Common variants at CDKAL1 and KLF9 are associated with body mass index in east Asian populations. 22344221 2012
dbSNP: rs1799923
rs1799923
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C0038436
Disease:
Post-Traumatic Stress Disorder 		0.010 GeneticVariation BEFREE These data offer preliminary evidence supporting an association between the rs1799923 polymorphism in the CCK gene and PTSD. 26454231 2015
dbSNP: rs1799923
rs1799923
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C0030319
Disease:
Panic Disorder 		0.010 GeneticVariation BEFREE The promoter variant (-36C > T; rs1799923) and an intron 1 polymorphism (IVS1-7C > G; rs754635) in the CCK gene were found to protect against PD (P<0.05). 20023595 2010
dbSNP: rs754635
rs754635
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C0030319
Disease:
Panic Disorder 		0.010 GeneticVariation BEFREE The promoter variant (-36C > T; rs1799923) and an intron 1 polymorphism (IVS1-7C > G; rs754635) in the CCK gene were found to protect against PD (P<0.05). 20023595 2010
dbSNP: rs554073050
rs554073050
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C2267227
Disease:
Bulimia Nervosa 		0.010 GeneticVariation BEFREE Therefore, the CC type of GHSR gene polymorphism (171T/C) is a risk factor for BN, but not for AN. 16362631 2006
dbSNP: rs554073050
rs554073050
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C0013473
Disease:
Eating Disorders 		0.010 GeneticVariation BEFREE In the present study, we examined the 171T/C polymorphism of the ghrelin receptor (growth hormone secretagogue receptor, GHSR) gene in patients diagnosed with EDs, because the subjects having ghrelin gene polymorphism (Leu72Met) was not detected in a Japanese population, previously. 16362631 2006
dbSNP: rs554073050
rs554073050
Entrez Id: 885
Gene Symbol: CCK
CCK
CUI: C0003125
Disease:
Anorexia Nervosa 		0.010 GeneticVariation BEFREE Therefore, the CC type of GHSR gene polymorphism (171T/C) is a risk factor for BN, but not for AN. 16362631 2006