Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs768048563
rs768048563
CACNA1A
0.010 GeneticVariation BEFREE The R689Q mutation was identified in a family in which FHM and benign familial infantile convulsions partially cosegregate. 12953268

2003