Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs202126574
rs202126574
Entrez Id: 10243;145226
Gene Symbol: GPHN;RDH12
GPHN;RDH12
CUI: C0035334
Disease:
Retinitis Pigmentosa
T 0.700 CausalMutation CLINVAR