{{Rsnum
|rsid=121912575
|Chromosome=6
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=TNXB
|position=32084536
|Gene_s=TNXB
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=600985
|rsnum=121912575
|variant=0004
}}{{ClinVar
|rsid=121912575
|Reversed=1
|FwdREF=G
|FwdALT=A
|REF=C
|ALT=T
|RSPOS=32052313
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=TNXB:7148
|GENE_NAME=TNXB
|GENE_ID=7148
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.32052313C>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=600985.0004
|CLNSIG=5
|CLNCUI=C0268337
|CLNDBN=Ehlers-Danlos syndrome, type 3
|Disease=Ehlers-Danlos syndrome
|CLNACC=RCV000009083.1
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=NBK1279:C0268337:130020:285:30652003
}}