Disease: Lesch-Nyhan Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs137852503
rs137852503
Entrez Id: 3251
Gene Symbol: HPRT1
HPRT1
CUI: C0023374
Disease:
Lesch-Nyhan Syndrome 		A 0.700 CausalMutation CLINVAR