HOXA1, homeobox A1, 3198

N. diseases: 95; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894018
rs104894018
Entrez Id: 3198;100506311
Gene Symbol: HOXA1;HOTAIRM1
HOXA1;HOTAIRM1
CUI: C1832215
Disease:
Athabaskan brainstem dysgenesis
A 0.700 CausalMutation CLINVAR
dbSNP: rs769152039
rs769152039
Entrez Id: 3198;100506311
Gene Symbol: HOXA1;HOTAIRM1
HOXA1;HOTAIRM1
CUI: C1832215
Disease:
Athabaskan brainstem dysgenesis
AC 0.700 CausalMutation CLINVAR