Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs369867819
rs369867819
Entrez Id: 2615;107984360
Gene Symbol: LRRC32;LOC107984360
LRRC32;LOC107984360
CUI: C0344290
Disease:
Vitreoretinal degeneration
A 0.700 GeneticVariation CLINVAR