{{Rsnum
|rsid=398122828
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=COL11A1
|position=102915630
|Gene_s=COL11A1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=T
|CHROM=1
|CLNACC=RCV000032995.26
|CLNALLE=1
|CLNDBN=Marshall syndrome
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0265235:154780:ORPHA560:33410002
|CLNHGVS=NC_000001.11:g.102915630C>T
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_080629.2:c.3852+1G>A; 120280.0012
|Disease=Marshall syndrome
|FwdALT=A
|FwdREF=G
|GENEINFO=COL11A1:1301
|GENE_ID=1301
|GENE_NAME=COL11A1
|REF=C
|RSPOS=102915630
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;DSS;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060100005000002110100
|WGT=1
|dbSNPBuildID=138
|rsid=398122828
|CLNORIGIN=1
}}