{{Rsnum
|rsid=121913129
|Chromosome=4
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=MSX1
|position=4862836
|Gene_s=MSX1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=142983
|rsnum=121913129
|variant=0001
}}{{ClinVar
|rsid=121913129
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=4864563
|CHROM=4
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=MSX1:4487
|GENE_NAME=MSX1
|GENE_ID=4487
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000004.11:g.4864563G>C
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=142983.0001
|CLNSIG=5
|CLNCUI=C0020608
|CLNDBN=Partial congenital absence of teeth
|Disease=Partial congenital absence of teeth
|CLNACC=RCV000016008.24
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0020608:106600:99798:64969001
}}