{{Rsnum
|rsid=104893635
|Chromosome=2
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=HOXD13
|position=176094672
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=HOXD13
}}{{omim
|id=142989
|rsnum=104893635
|variant=0009
}}{{ClinVar
|rsid=104893635
|Reversed=0
|FwdREF=A
|FwdALT=G
|REF=A
|ALT=G
|RSPOS=176959400
|CHROM=2
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=HOXD13:3239
|GENE_NAME=HOXD13
|GENE_ID=3239
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.176959400A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=142989.0009
|CLNSIG=5
|CLNCUI=C1861348; C0268151
|CLNDBN=Syndactyly type 5
|Disease=Syndactyly type 5
|CLNACC=RCV000016002.24
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1861348:186300:93406
}}