rs137853013

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs137853013(C;T)

Make rs137853013(T;T)

Reference

GRCh38 38.1/141

Chromosome

3

Position

130969385

Gene

ATP2C1

is a	snp
is	mentioned by
dbSNP	rs137853013
dbSNP (classic)	rs137853013
ClinGen	rs137853013
ebi	rs137853013
HLI	rs137853013
Exac	rs137853013
Gnomad	rs137853013
Varsome	rs137853013
LitVar	rs137853013
Map	rs137853013
PheGenI	rs137853013
Biobank	rs137853013
1000 genomes	rs137853013
hgdp	rs137853013
ensembl	rs137853013
geneview	rs137853013
scholar	rs137853013
google	rs137853013
pharmgkb	rs137853013
gwascentral	rs137853013
openSNP	rs137853013
23andMe	rs137853013
SNPshot	rs137853013
SNPdbe	rs137853013
MSV3d	rs137853013
GWAS Ctlg	rs137853013

Max Magnitude

0

OMIM	604384
Desc
Variant	0003
Related	also

ClinVar
Risk	rs137853013(G;G) rs137853013(T;T)
Alt	rs137853013(G;G) rs137853013(T;T)
Reference	Rs137853013(C;C)
Significance	Pathogenic
Disease	Familial benign pemphigus
Variation	info
Gene	ATP2C1
CLNDBN	Familial benign pemphigus
Reversed	0
HGVS	NC_000003.11:g.130688229C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000005925.2,