{{Rsnum
|rsid=121918010
|Chromosome=1
|Orientation=plus
|geno1=(C;C)
|geno2=(C;T)
|geno3=(T;T)
|Gene=ALPL
|position=21573781
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
|Gene_s=ALPL
}}{{omim
|id=171760
|rsnum=121918010
|variant=0011
}}{{ClinVar
|rsid=121918010
|Reversed=0
|FwdREF=T
|FwdALT=C
|REF=T
|ALT=C
|RSPOS=21573781
|CHROM=1
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000a05000002110100
|GENEINFO=ALPL:249
|GENE_NAME=ALPL
|GENE_ID=249
|WGT=1
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000001.11:g.21573781T>C
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=NM_000478.4:c.979T>C; 171760.0011
|CLNSIG=5
|CLNCUI=C0268412
|CLNDBN=Infantile hypophosphatasia
|Disease=Infantile hypophosphatasia
|CLNACC=RCV000014664.24
|Tags=PM;S3D;NSM;REF;ASP;OTHERKG;LSD;OM
|CLNDSDB=GeneReviews:MedGen:OMIM:SNOMED_CT
|CLNDSDBID=NBK1150:C0268412:241500:55236002
}}