CCNQ, cyclin Q, 92002

N. diseases: 56; N. variants: 4
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs12010175
rs12010175
Entrez Id: 92002
Gene Symbol: CCNQ
CCNQ
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		G 0.800 GeneticVariation GWASCAT A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans. 22961080 2013
dbSNP: rs12010175
rs12010175
Entrez Id: 92002
Gene Symbol: CCNQ
CCNQ
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		G 0.800 GeneticVariation GWASDB A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans. 22961080 2013
dbSNP: rs1569536789
rs1569536789
Entrez Id: 92002
Gene Symbol: CCNQ
CCNQ
CUI: C2678045
Disease:
TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS 		T 0.700 CausalMutation CLINVAR
dbSNP: rs1569536891
rs1569536891
Entrez Id: 92002
Gene Symbol: CCNQ
CCNQ
CUI: C2678045
Disease:
TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS 		TA 0.700 CausalMutation CLINVAR
dbSNP: rs63749972
rs63749972
Entrez Id: 92002
Gene Symbol: CCNQ
CCNQ
CUI: C2678045
Disease:
TOE SYNDACTYLY, TELECANTHUS, AND ANOGENITAL AND RENAL MALFORMATIONS 		T 0.700 CausalMutation CLINVAR