{{Rsnum
|rsid=397514499
|Chromosome=19
|Orientation=minus
|geno1=(G;G)
|geno2=(G;T)
|geno3=(T;T)
|Gene=AP2S1
|position=46846102
|Gene_s=AP2S1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{ClinVar
|ALT=A,T
|CHROM=19
|CLNACC=RCV000032620.1; RCV000032621.1
|CLNALLE=1; 2
|CLNDBN=Hypocalciuric hypercalcemia, familial, type 3
|CLNDSDB=MedGen:OMIM:Orphanet
|CLNDSDBID=C1833372:600740:405
|CLNHGVS=NC_000019.9:g.47349359C>A; NC_000019.9:g.47349359C>T
|CLNSIG=5
|CLNSRC=OMIM Allelic Variant
|CLNSRCID=602242.0002; 602242.0003
|Disease=Hypocalciuric hypercalcemia
|FwdALT=A,T
|FwdREF=G
|GENEINFO=AP2S1:1175
|GENE_ID=1175
|GENE_NAME=AP2S1
|REF=C
|RSPOS=47349359
|Reversed=1
|SAO=0
|SSR=0
|Tags=RV;PM;OTHERKG;LSD;OM
|VC=SNV
|VP=0x050060000000000002110100
|WGT=0
|dbSNPBuildID=136
|rsid=397514499
}}