{{Rsnum
|rsid=387906325
|Chromosome=11
|position=44309669
|Orientation=minus
|geno1=(-;-)
|geno2=(-;TGCAAGACGC)
|geno3=(TGCAAGACGC;TGCAAGACGC)
|Gene=ALX4
|Gene_s=ALX4
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=G
|CHROM=11
|CLNACC=RCV000005322.2
|CLNALLE=1
|CLNDBN=Parietal foramina 2
|CLNDSDB=GeneReviews:MedGen:OMIM:Orphanet
|CLNDSDBID=NBK1128:C1865044:609597:60015
|CLNHGVS=NC_000011.9:g.44331219_44331228delGCGTCTTGCA
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=605420.0007
|Disease=Parietal foramina 2
|FwdREF=TGCAAGACGC
|REF=GGCGTCTTGCA
|RSPOS=44331218
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=DIV
|VP=0x050060000000000002110200
|WGT=0
|dbSNPBuildID=137
|rsid=387906325
|GENEINFO=ALX4:60529
|GENE_ID=60529
|GENE_NAME=ALX4
}}