HOXA2, homeobox A2, 3199

N. diseases: 26; N. variants: 3
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554334301
rs1554334301
Entrez Id: 3199
Gene Symbol: HOXA2
HOXA2
CUI: C4694002
Disease:
MICROTIA WITHOUT HEARING IMPAIRMENT 		A 0.700 CausalMutation CLINVAR
dbSNP: rs398122360
rs398122360
Entrez Id: 3199
Gene Symbol: HOXA2
HOXA2
CUI: C3808166
Disease:
MICROTIA WITH OR WITHOUT HEARING IMPAIRMENT 		A 0.700 CausalMutation CLINVAR
dbSNP: rs119489104
rs119489104
Entrez Id: 3199
Gene Symbol: HOXA2
HOXA2
CUI: C2676772
Disease:
Microtia, Hearing Impairment, And Cleft Palate 		T 0.800 CausalMutation CLINVAR
dbSNP: rs119489104
rs119489104
Entrez Id: 3199
Gene Symbol: HOXA2
HOXA2
CUI: C2676772
Disease:
Microtia, Hearing Impairment, And Cleft Palate 		0.800 GeneticVariation UNIPROT