{{Rsnum
|rsid=121912931
|Chromosome=6
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=COL9A1
|position=70281033
|Gene_s=COL9A1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=120210
|rsnum=121912931
|variant=0002
}}{{ClinVar
|rsid=121912931
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=70990736
|CHROM=6
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=COL9A1:1297
|GENE_NAME=COL9A1
|GENE_ID=1297
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000006.11:g.70990736G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=120210.0002
|CLNSIG=5
|CLNCUI=C1852831
|CLNDBN=Stickler syndrome, type 4
|Disease=Stickler syndrome
|CLNACC=RCV000018735.22
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet:Orphanet
|CLNDSDBID=NBK1302:C1852831:614134:250984:828
}}