{{Rsnum
|rsid=119489104
|Chromosome=7
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=HOXA2
|position=27101301
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HOXA2
}}{{omim
|id=604685
|rsnum=119489104
|variant=0001
}}{{ClinVar
|rsid=119489104
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=27140920
|CHROM=7
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HOXA2:3199
|GENE_NAME=HOXA2
|GENE_ID=3199
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000007.13:g.27140920G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604685.0001
|CLNSIG=5
|CLNCUI=C2676772
|CLNDBN=Microtia, hearing impairment, and cleft palate
|Disease=Microtia
|CLNACC=RCV000005738.3
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C2676772:612290:140963
}}