{{Rsnum
|rsid=121918215
|Chromosome=2
|Orientation=minus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=OBSL1
|position=219568188
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=OBSL1
}}{{omim
|id=610991
|rsnum=121918215
|variant=0002
}}{{ClinVar
|rsid=121918215
|Reversed=1
|FwdREF=C
|FwdALT=A
|REF=G
|ALT=T
|RSPOS=220432910
|CHROM=2
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110100
|GENEINFO=OBSL1:23363
|GENE_NAME=OBSL1
|GENE_ID=23363
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000002.11:g.220432910G>T
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=610991.0002
|CLNSIG=5
|CLNCUI=C2752041
|CLNDBN=Three M syndrome 2
|Disease=Three M syndrome 2
|CLNACC=RCV000001101.2
|Tags=RV;PM;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1481:C2752041:612921:2616
}}