Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs771054395
rs771054395
Entrez Id: 84100
Gene Symbol: ARL6
ARL6
CUI: C0035334
Disease:
Retinitis Pigmentosa
C 0.700 GeneticVariation CLINVAR Novel homozygous mutations in the genes ARL6 and BBS10 underlying Bardet-Biedl syndrome. 23219996 2013