{{Rsnum
|rsid=104894192
|Chromosome=11
|Orientation=minus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ALX4
|position=44275389
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALX4
}}{{omim
|id=605420
|rsnum=104894192
|variant=0002
}}{{ClinVar
|rsid=104894192
|Reversed=1
|FwdREF=C
|FwdALT=T
|REF=G
|ALT=A
|RSPOS=44296939
|CHROM=11
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ALX4:60529
|GENE_NAME=ALX4
|GENE_ID=60529
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000011.9:g.44296939G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=605420.0002
|CLNSIG=5
|CLNCUI=C1865044
|CLNDBN=Parietal foramina 2
|Disease=Parietal foramina 2
|CLNACC=RCV000005317.1
|Tags=RV;PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1128:C1865044:609597:60015
}}