Disease: Bardet-Biedl Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893678
rs104893678
Entrez Id: 84100
Gene Symbol: ARL6
ARL6
CUI: C0752166
Disease:
Bardet-Biedl Syndrome 		T 0.700 CausalMutation CLINVAR
dbSNP: rs771054395
rs771054395
Entrez Id: 84100
Gene Symbol: ARL6
ARL6
CUI: C0752166
Disease:
Bardet-Biedl Syndrome 		0.010 GeneticVariation BEFREE Sequence analysis revealed a novel homozygous missense mutation (c.281T>C, p.Ile94Thr) in the gene ARL6 in family A and a nonsense mutation (c.1075C>T, p.Gln359*) in the gene BBS10 in family B. Mutations identified in the present study extend the body of evidence implicating the genes ARL6 and BBS10 in causing Bardet-Biedl syndrome. 23219996 2013
dbSNP: rs771054395
rs771054395
Entrez Id: 84100
Gene Symbol: ARL6
ARL6
CUI: C0752166
Disease:
Bardet-Biedl Syndrome 		0.010 GeneticVariation BEFREE Sequence analysis revealed a novel homozygous missense mutation (c.281T>C, p.Ile94Thr) in the gene ARL6 in family A and a nonsense mutation (c.1075C>T, p.Gln359*) in the gene BBS10 in family B. Mutations identified in the present study extend the body of evidence implicating the genes ARL6 and BBS10 in causing Bardet-Biedl syndrome. 23219996 2013