{{Rsnum
|rsid=104893634
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=HOXD10
|position=176119164
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HOXD10
}}{{omim
|id=142984
|rsnum=104893634
|variant=0001
}}{{ClinVar
|rsid=104893634
|Reversed=0
|FwdREF=T
|FwdALT=A
|REF=T
|ALT=A
|RSPOS=176983892
|CHROM=2
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HOXD10:3236
|GENE_NAME=HOXD10
|GENE_ID=3236
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.176983892T>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=142984.0001
|CLNSIG=5
|CLNCUI=C0240912
|CLNDBN=Vertical talus, congenital; Charcot-Marie-Tooth disease, foot deformity of
|Disease=Vertical talus; Charcot-Marie-Tooth disease
|CLNACC=RCV000016006.24; RCV000016007.20
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet; MedGen
|CLNDSDBID=C0240912:192950:178382; C1840503
}}