{{Rsnum
|rsid=121908166
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ALX3
|position=110061550
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALX3
}}{{omim
|id=606014
|rsnum=121908166
|variant=0002
}}{{ClinVar
|rsid=121908166
|Reversed=1
|FwdREF=A
|FwdALT=G
|REF=T
|ALT=C
|RSPOS=110061550
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=ALX3:257
|GENE_NAME=ALX3
|GENE_ID=257
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.110061550T>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_006492.2:c.608A>G; 606014.0002
|CLNSIG=5
|CLNCUI=C1876203
|CLNDBN=Frontonasal dysplasia
|Disease=Frontonasal dysplasia
|CLNACC=RCV000004906.1
|Tags=RV;PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1876203:136760
}}