Source: CLINVAR

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909076
rs121909076
TULP1
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		G 0.700 CausalMutation CLINVAR

dbSNP: rs1554125752
rs1554125752
TULP1
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		CG 0.700 GeneticVariation CLINVAR

dbSNP: rs527236117
rs527236117
TULP1
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		T 0.700 GeneticVariation CLINVAR