{{Rsnum
|rsid=137853012
|Chromosome=3
|Orientation=plus
|geno1=(A;A)
|geno2=(A;G)
|geno3=(G;G)
|Gene=ATP2C1
|position=130963981
|Gene_s=ATP2C1
|Assembly=GRCh38
|GenomeBuild=38.1
|dbSNPBuild=141
}}{{omim
|id=604384
|variant=0002
|rsnum=137853012
}}{{ClinVar
|rsid=137853012
|Reversed=0
|FwdREF=G
|FwdALT=A
|REF=G
|ALT=A
|RSPOS=130682825
|CHROM=3
|dbSNPBuildID=133
|SSR=0
|SAO=1
|VP=0x050260000000000002110100
|GENEINFO=ATP2C1:27032
|GENE_NAME=ATP2C1
|GENE_ID=27032
|WGT=0
|VC=SNV
|CLNALLE=1
|CLNHGVS=NC_000003.11:g.130682825G>A
|CLNSRC=OMIM Allelic Variant
|CLNORIGIN=1
|CLNSRCID=604384.0002
|CLNSIG=5
|CLNCUI=C0085106
|CLNDBN=Familial benign pemphigus
|Disease=Familial benign pemphigus
|CLNACC=RCV000005924.1
|Tags=PM;S3D;OTHERKG;LSD;OM
|CLNDSDB=MedGen:OMIM:Orphanet:SNOMED_CT
|CLNDSDBID=C0085106:169600:2841:79468000
}}