{{Rsnum
|rsid=121908169
|Chromosome=1
|Orientation=minus
|geno1=(A;A)
|geno2=(A;T)
|geno3=(T;T)
|Gene=ALX3
|position=110064638
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALX3
}}{{omim
|id=606014
|rsnum=121908169
|variant=0005
}}{{ClinVar
|rsid=121908169
|Reversed=1
|FwdREF=T
|FwdALT=A
|REF=A
|ALT=T
|RSPOS=110064638
|CHROM=1
|dbSNPBuildID=132
|SSR=0
|SAO=1
|VP=0x050260000605000002110100
|GENEINFO=ALX3:257
|GENE_NAME=ALX3
|GENE_ID=257
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.110064638A>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_006492.2:c.543T>A; 606014.0005
|CLNSIG=5
|CLNCUI=C1876203
|CLNDBN=Frontonasal dysplasia
|Disease=Frontonasal dysplasia
|CLNACC=RCV000004909.1
|Tags=RV;PM;S3D;NSN;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM
|CLNDSDBID=C1876203:136760
}}