Source: CLINVAR ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1387102485
rs1387102485
Entrez Id: 6094;256364
Gene Symbol: ROM1;EML3
ROM1;EML3
CUI: C2675552
Disease:
Retinitis Pigmentosa 7, Digenic 		TG 0.700 CausalMutation CLINVAR
dbSNP: rs768652143
rs768652143
Entrez Id: 6094;256364
Gene Symbol: ROM1;EML3
ROM1;EML3
CUI: C0035334
Disease:
Retinitis Pigmentosa 		T 0.700 GeneticVariation CLINVAR