{{Rsnum
|rsid=121912971
|Chromosome=5
|Orientation=plus
|geno1=(GC;GC)
|geno2=(GC;TA)
|geno3=(TA;TA)
|Gene=MSX2
|position=174724924
|Gene_s=MSX2
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=123101
|rsnum=121912971
|variant=0005
}}{{ClinVar
|rsid=121912971
|Reversed=0
|FwdREF=GC
|FwdALT=TA
|REF=AGC
|ALT=ATA
|RSPOS=174151926
|CHROM=5
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050060000000000002110800
|GENEINFO=MSX2:4488
|GENE_NAME=MSX2
|GENE_ID=4488
|WGT=0
|VC=MNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.174151927_174151928delGCinsTA
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=123101.0005
|CLNSIG=5
|CLNCUI=C1868599
|CLNDBN=Parietal foramina 1
|Disease=Parietal foramina 1
|CLNACC=RCV000018478.22
|Tags=PM;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1868599
}}