Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387907136
rs387907136
C8orf37 ; C8orf37-AS1
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs387907137
rs387907137
C8orf37 ; C8orf37-AS1
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		C 0.700 CausalMutation CLINVAR