{{Rsnum
|rsid=139073416
|Chromosome=1
|Orientation=plus
|geno1=(A;A)
|geno2=(A;C)
|geno3=(C;C)
|Gene=PIGV
|position=26795056
|Gene_s=PIGV
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,T
|CHROM=1
|CLNACC=RCV000001347.2; RCV000001350.1
|CLNALLE=1; 2
|CLNDBN=Hyperphosphatasia with mental retardation syndrome 1
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1855923:239300:ORPHA247262
|CLNHGVS=NC_000001.11:g.26795056C>A; NC_000001.11:g.26795056C>T
|CLNSIG=5
|CLNSRC=ClinVar; OMIM Allelic Variant
|CLNSRCID=NM_017837.3:c.1022C>A; 610274.0001; NM_017837.3:c.1022C>T; 610274.0004
|Disease=Hyperphosphatasia with mental retardation syndrome 1
|FwdALT=A,T
|FwdREF=C
|GENEINFO=PIGV:55650
|GENE_ID=55650
|GENE_NAME=PIGV
|REF=C
|RSPOS=26795056
|Reversed=0
|SAO=0
|SSR=0
|Tags=PM;NSM;REF;ASP;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000a05000002110100
|WGT=1
|dbSNPBuildID=134
|rsid=139073416
|CLNORIGIN=1
}}