Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555550617
rs1555550617
Entrez Id: 10594
Gene Symbol: PRPF8
PRPF8
CUI: C0035334
Disease:
Retinitis Pigmentosa
T 0.700 GeneticVariation CLINVAR