Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906971
rs387906971
Entrez Id: 10594
Gene Symbol: PRPF8
PRPF8
CUI: C1838702
Disease:
Retinitis Pigmentosa 13
A 0.700 CausalMutation CLINVAR