{{Rsnum
|rsid=121909352
|Chromosome=8
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=GDF6
|position=96145185
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=GDF6
}}{{omim
|id=601147
|rsnum=121909352
|variant=0001
}}{{ClinVar
|rsid=121909352
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=97157413
|CHROM=8
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=GDF6:392255
|GENE_NAME=GDF6
|GENE_ID=392255
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000008.10:g.97157413G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=601147.0001
|CLNSIG=5
|CLNCUI=C1861689; C2751307
|CLNDBN=Klippel-Feil syndrome 1, autosomal dominant; Microphthalmia, isolated 4; Leber congenital amaurosis 17
|Disease=Klippel-Feil syndrome 1; Microphthalmia; Leber congenital amaurosis 17
|CLNACC=RCV000008876.2; RCV000008877.2; RCV000054424.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1861689:118100:2345; C2751307:613094:2542; CN178541:615360:65
}}