rs79891110, CACNA1C

N. diseases: 6
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Syndactyly
CUI: C0039075
Disease: Syndactyly
0.010 GeneticVariation BEFREE The proband with severe syndactyly and delayed language skills was identified harboring a G406R mutation in CACNA1C. 23580742 2013