Source: CLINVAR ×
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1057516850
rs1057516850
HEXA
T 0.700 CausalMutation CLINVAR

dbSNP: rs1057516850
rs1057516850
HEXA
T 0.700 GeneticVariation CLINVAR