{{Rsnum
|rsid=387906737
|Chromosome=7
|position=97022192
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=DLX5
|Gene_s=DLX5
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=7
|CLNACC=RCV000022921.2
|CLNALLE=1
|CLNDBN=Split-hand/foot malformation 1 with sensorineural hearing loss
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1857344:220600:71271
|CLNHGVS=NC_000007.13:g.96651504T>G
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=600028.0001
|Disease=Split-hand/foot malformation 1 with sensorineural hearing loss
|FwdALT=C
|FwdREF=A
|REF=T
|RSPOS=96651504
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=137
|rsid=387906737
|GENEINFO=DLX5:1749
|GENE_ID=1749
|GENE_NAME=DLX5
}}