{{Rsnum
|rsid=121912972
|Chromosome=5
|Orientation=plus
|geno1=(-;-)
|geno2=(-;G)
|geno3=(G;G)
|Gene=MSX2
|position=174725004
|Gene_s=MSX2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=123101
|rsnum=121912972
|variant=0006
}}{{ClinVar
|rsid=121912972
|Reversed=0
|FwdREF=G
|FwdALT=
|REF=TG
|ALT=T
|RSPOS=174152005
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110200
|GENEINFO=MSX2:4488
|GENE_NAME=MSX2
|GENE_ID=4488
|WGT=0
|VC=DIV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.174152007delG
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=123101.0006
|CLNSIG=5
|CLNCUI=C1868599
|CLNDBN=Parietal foramina 1
|Disease=Parietal foramina 1
|CLNACC=RCV000018479.22
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1868599
}}