{{Rsnum
|rsid=63751220
|Chromosome=8
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=GDF6
|position=96145065
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GDF6
}}{{omim
|id=601147
|rsnum=63751220
|variant=0002
}}

{{omim
|id=118100
|rsnum=63751220
}}

{{ClinVar
|rsid=63751220
|Reversed=1
|FwdREF=T
|FwdALT=C
|REF=A
|ALT=G
|RSPOS=97157293
|CHROM=8
|dbSNPBuildID=130
|SSR=0
|SAO=1
|VP=0x050068000000000002110100
|GENEINFO=GDF6:392255
|GENE_NAME=GDF6
|GENE_ID=392255
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.97157293A>G
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601147.0002
|CLNSIG=5
|CLNCUI=C1861689
|CLNDBN=Klippel-Feil syndrome 1, autosomal dominant
|Disease=Klippel-Feil syndrome 1
|CLNACC=RCV000008878.1
|Tags=RV;PM;PMC;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1861689:118100:2345
}}

{{PMID|18425797}} Mutations in GDF6 are associated with vertebral segmentation defects in Klippel-Feil syndrome.

{{on chip | 23andMe v3}}
{{on chip | 23andMe v4}}