RNF6, ring finger protein 6, 6049

N. diseases: 46; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10507349
rs10507349
Entrez Id: 6049
Gene Symbol: RNF6
RNF6
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		G 0.800 GeneticVariation GWASCAT Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population. 30718926 2019
dbSNP: rs10507349
rs10507349
Entrez Id: 6049
Gene Symbol: RNF6
RNF6
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		G 0.800 GeneticVariation GWASCAT Identification of new susceptibility loci for type 2 diabetes and shared etiological pathways with coronary heart disease. 28869590 2017
dbSNP: rs10507349
rs10507349
Entrez Id: 6049
Gene Symbol: RNF6
RNF6
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		G 0.800 GeneticVariation GWASDB Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. 24509480 2014
dbSNP: rs10507349
rs10507349
Entrez Id: 6049
Gene Symbol: RNF6
RNF6
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		G 0.800 GeneticVariation GWASCAT Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility. 24509480 2014
dbSNP: rs121434522
rs121434522
Entrez Id: 6049
Gene Symbol: RNF6
RNF6
CUI: C4016881
Disease:
ESOPHAGEAL SQUAMOUS CELL CARCINOMA, SOMATIC 		T 0.700 CausalMutation CLINVAR
dbSNP: rs121434523
rs121434523
Entrez Id: 6049
Gene Symbol: RNF6
RNF6
CUI: C4016881
Disease:
ESOPHAGEAL SQUAMOUS CELL CARCINOMA, SOMATIC 		T 0.700 CausalMutation CLINVAR
dbSNP: rs121434524
rs121434524
Entrez Id: 6049
Gene Symbol: RNF6
RNF6
CUI: C4016881
Disease:
ESOPHAGEAL SQUAMOUS CELL CARCINOMA, SOMATIC 		T 0.700 CausalMutation CLINVAR