Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886041715
rs886041715
C 0.700 GeneticVariation CLINVAR

dbSNP: rs587777057
rs587777057
0.010 GeneticVariation BEFREE GNAO1-associated epileptic encephalopathy and movement disorders: c.607G>A variant represents a probable mutation hotspot with a distinct phenotype. 28202424

2017