Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894578
rs104894578
KCNJ2
CUI: C4551485
Disease: Clinodactyly
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