{{Rsnum
|rsid=104893853
|Chromosome=4
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=MSX1
|position=4862854
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MSX1
}}{{omim
|id=142983
|rsnum=104893853
|variant=0003
}}{{ClinVar
|rsid=104893853
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=4864581
|CHROM=4
|dbSNPBuildID=132
|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.4864581C>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=142983.0003
|CLNSIG=5
|CLNCUI=C0406735
|CLNDBN=Hypoplastic enamel-onycholysis-hypohidrosis syndrome
|Disease=Hypoplastic enamel-onycholysis-hypohidrosis syndrome
|CLNACC=RCV000016011.24
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0406735:189500:2228:400036004
}}