{{Rsnum
|rsid=121918001
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ALPL
|position=21561126
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALPL
}}{{omim
|id=171760
|rsnum=121918001
|variant=0002
}}{{ClinVar
|rsid=121918001
|Reversed=0
|FwdREF=C
|FwdALT=T
|REF=C
|ALT=T
|RSPOS=21561126
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260080a05000002110100
|GENEINFO=ALPL:249
|GENE_NAME=ALPL
|GENE_ID=249
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.21561126C>T
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000478.4:c.211C>T; NM_001177520.1:c.66+381C>T; 171760.0002
|CLNSIG=5
|CLNCUI=C0268412
|CLNDBN=Infantile hypophosphatasia
|Disease=Infantile hypophosphatasia
|CLNACC=RCV000014649.24
|Tags=PM;S3D;NSM;REF;INT;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1150:C0268412:241500:55236002
}}