Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs61755792
rs61755792
PRPH2
CUI: C0024437
Disease: Macular degeneration
Macular degeneration 		0.020 GeneticVariation BEFREE Insights into the mechanisms of macular degeneration associated with the R172W mutation in RDS. 24463884

2014
dbSNP: rs61755792
rs61755792
PRPH2
CUI: C0024437
Disease: Macular degeneration
Macular degeneration 		0.020 GeneticVariation BEFREE One mutation in exon 1, R172W, has been described previously in other ethnic groups as causing a macular degeneration. 10193525

1998