{{Rsnum
|rsid=121918003
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;G)
|geno3=(G;G)
|Gene=ALPL
|position=21561127
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALPL
}}{{omim
|id=171760
|rsnum=121918003
|variant=0004
}}{{ClinVar
|rsid=121918003
|Reversed=0
|FwdREF=G
|FwdALT=C
|REF=G
|ALT=C
|RSPOS=21561127
|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.21561127G>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000478.4:c.212G>C; NM_001177520.1:c.66+382G>C; 171760.0004
|CLNSIG=5
|CLNCUI=C0268412
|CLNDBN=Infantile hypophosphatasia
|Disease=Infantile hypophosphatasia
|CLNACC=RCV000014653.18
|Tags=PM;S3D;NSM;REF;INT;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1150:C0268412:241500:55236002
}}