{{Rsnum
|rsid=104893896
|Chromosome=5
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=MSX2
|position=174729294
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MSX2
}}{{omim
|id=123101
|rsnum=104893896
|variant=0003
}}{{ClinVar
|rsid=104893896
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=174156297
|CHROM=5
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MSX2:4488
|GENE_NAME=MSX2
|GENE_ID=4488
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.174156297G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=123101.0003
|CLNSIG=5
|CLNCUI=C1868599
|CLNDBN=Parietal foramina 1
|Disease=Parietal foramina 1
|CLNACC=RCV000018476.26
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen
|CLNDSDBID=C1868599
}}