Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs878853387
rs878853387
Entrez Id: 10594
Gene Symbol: PRPF8
PRPF8
CUI: C0854723
Disease:
Retinal Dystrophies
G 0.700 GeneticVariation CLINVAR