Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs140366557
rs140366557
IFT43
A 0.800 GeneticVariation CLINVAR A mutation in IFT43 causes non-syndromic recessive retinal degeneration. 28973684

2017
dbSNP: rs140366557
rs140366557
IFT43
0.800 GeneticVariation UNIPROT A mutation in IFT43 causes non-syndromic recessive retinal degeneration. 28973684

2017