Source: BEFREE

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs62645944
rs62645944
ABCA4
CUI: C0035334
Disease: Retinitis Pigmentosa
Retinitis Pigmentosa 		0.710 GeneticVariation BEFREE Another patient in this family with a severe type of retinitis pigmentosa (RP) carried the 768G-->T mutation homozygously. 15019334

2004