Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6633421
rs6633421
Entrez Id: 22866
Gene Symbol: CNKSR2
CNKSR2
CUI: C0011860
Disease:
Diabetes Mellitus, Non-Insulin-Dependent 		A 0.700 GeneticVariation GWASCAT Identification of 28 new susceptibility loci for type 2 diabetes in the Japanese population. 30718926 2019
dbSNP: rs1569161831
rs1569161831
Entrez Id: 22866
Gene Symbol: CNKSR2
CNKSR2
CUI: C0025362
Disease:
Mental Retardation 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1569261319
rs1569261319
Entrez Id: 22866
Gene Symbol: CNKSR2
CNKSR2
CUI: C4538788
Disease:
MENTAL RETARDATION, X-LINKED, SYNDROMIC, HOUGE TYPE 		A 0.700 CausalMutation CLINVAR
dbSNP: rs606231282
rs606231282
Entrez Id: 22866
Gene Symbol: CNKSR2
CNKSR2
CUI: C4538788
Disease:
MENTAL RETARDATION, X-LINKED, SYNDROMIC, HOUGE TYPE 		CA 0.700 CausalMutation CLINVAR
dbSNP: rs771705122
rs771705122
Entrez Id: 22866
Gene Symbol: CNKSR2
CNKSR2
CUI: C0009402
Disease:
Colorectal Carcinoma 		0.700 GeneticVariation UNIPROT
dbSNP: rs904072058
rs904072058
Entrez Id: 22866
Gene Symbol: CNKSR2
CNKSR2
CUI: C4538788
Disease:
MENTAL RETARDATION, X-LINKED, SYNDROMIC, HOUGE TYPE 		T 0.700 CausalMutation CLINVAR