{{Rsnum
|rsid=121918007
|Gene=ALPL
|Chromosome=1
|position=21564139
|Orientation=plus
|GMAF=0.001377
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene_s=ALPL
}}{{omim
|id=171760
|rsnum=121918007
|variant=0008
}}{{ClinVar
|rsid=121918007
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=21564139
|CHROM=1
|GMAF=0.0014
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000016110100
|GENEINFO=ALPL:249
|GENE_NAME=ALPL
|GENE_ID=249
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.21564139G>A
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000478.4:c.571G>A; 171760.0008
|CLNSIG=5
|CLNCUI=C0268412; C0220743; C0268413
|CLNDBN=Infantile hypophosphatasia; Childhood hypophosphatasia; Adult hypophosphatasia
|Disease=Infantile hypophosphatasia; Childhood hypophosphatasia; Adult hypophosphatasia
|CLNACC=RCV000014658.24; RCV000014659.23; RCV000014660.24
|Tags=PM;S3D;NSM;REF;ASP;KGPhase1;KGPROD;OTHERKG;LSD;OM
|CAF=0.9986; 0.001377
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1150:C0268412:241500:55236002; NBK1150:C0220743:241510:30174008; NBK1150:C0268413:146300:20756002
|COMMON=1
}}