Disease: Clinodactyly ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894578
rs104894578
Entrez Id: 3759
Gene Symbol: KCNJ2
KCNJ2
CUI: C4551485
Disease:
Clinodactyly 		0.010 GeneticVariation BEFREE Three relatives had clinodactyly as the only manifestation but the R218W mutation was absent, suggesting that this characteristic may be influenced by another gene. 17119796 2006