rs74085882

Orientation

plus

Stabilized

plus

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

Make rs74085882(C;C)

Make rs74085882(C;T)

Reference

GRCh38 38.1/141

Chromosome

13

Position

51944251

Gene

ATP7B

is a	snp
is	mentioned by
dbSNP	rs74085882
dbSNP (classic)	rs74085882
ClinGen	rs74085882
ebi	rs74085882
HLI	rs74085882
Exac	rs74085882
Gnomad	rs74085882
Varsome	rs74085882
LitVar	rs74085882
Map	rs74085882
PheGenI	rs74085882
Biobank	rs74085882
1000 genomes	rs74085882
hgdp	rs74085882
ensembl	rs74085882
geneview	rs74085882
scholar	rs74085882
google	rs74085882
pharmgkb	rs74085882
gwascentral	rs74085882
openSNP	rs74085882
23andMe	rs74085882
SNPshot	rs74085882
SNPdbe	rs74085882
MSV3d	rs74085882
GWAS Ctlg	rs74085882

GMAF

0.001377

Max Magnitude

0

ClinVar
Risk	rs74085882(C;C)
Alt	rs74085882(C;C)
Reference	Rs74085882(T;T)
Significance	Other
Disease	Wilson disease not specified
Variation	info
Gene	ATP7B
CLNDBN	Wilson disease not specified
Reversed	0
HGVS	NC_000013.10:g.52518387T>C
CLNSRC	ClinVar LabCorp University of Washington
CLNACC	RCV000029368.3, RCV000244000.2,