{{Rsnum
|rsid=387907023
|Chromosome=1
|position=26794501
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=PIGV
|Gene_s=PIGV
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A
|CHROM=1
|CLNACC=RCV000023806.1
|CLNALLE=1
|CLNDBN=Hyperphosphatasia with mental retardation syndrome 1
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1855923:239300:ORPHA247262
|CLNHGVS=NC_000001.11:g.26794501G>A
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_017837.3:c.467G>A; 610274.0005
|Disease=Hyperphosphatasia with mental retardation syndrome 1
|FwdALT=A
|FwdREF=G
|REF=G
|RSPOS=26794501
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000a05000002110100
|WGT=1
|dbSNPBuildID=137
|rsid=387907023
|GENEINFO=PIGV:55650
|GENE_ID=55650
|GENE_NAME=PIGV
|CLNORIGIN=1
}}