Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886039909
rs886039909
Entrez Id: 3339
Gene Symbol: HSPG2
HSPG2
CUI: C0005744
Disease:
Blepharophimosis
T 0.700 GeneticVariation CLINVAR