{{Rsnum
|rsid=104893895
|Chromosome=5
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=MSX2
|position=174729222
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=MSX2
}}{{omim
|id=123101
|rsnum=104893895
|variant=0001
}}{{ClinVar
|rsid=104893895
|Reversed=0
|FwdREF=C
|FwdALT=A
|REF=C
|ALT=A
|RSPOS=174156225
|CHROM=5
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050368000000000002110100
|GENEINFO=MSX2:4488
|GENE_NAME=MSX2
|GENE_ID=4488
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000005.9:g.174156225C>A
|CLNSRC=GeneReviews; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NBK1128; 123101.0001
|CLNSIG=5
|CLNCUI=C1858160
|CLNDBN=Craniosynostosis 2
|Disease=Craniosynostosis 2
|CLNACC=RCV000018474.27
|Tags=PM;PMC;S3D;SLO;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1128:C1858160:604757:1541
}}{{PMID Auto
|PMID=16319823
|Title=Enlarged parietal foramina caused by mutations in the homeobox genes ALX4 and MSX2: from genotype to phenotype.
|OA=1
}}