rs367956522

Orientation

plus

Stabilized

plus

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

Make rs367956522(C;C)

Make rs367956522(C;T)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

51949798

Gene

ATP7B

is a	snp
is	mentioned by
dbSNP	rs367956522
dbSNP (classic)	rs367956522
ClinGen	rs367956522
ebi	rs367956522
HLI	rs367956522
Exac	rs367956522
Gnomad	rs367956522
Varsome	rs367956522
LitVar	rs367956522
Map	rs367956522
PheGenI	rs367956522
Biobank	rs367956522
1000 genomes	rs367956522
hgdp	rs367956522
ensembl	rs367956522
geneview	rs367956522
scholar	rs367956522
google	rs367956522
pharmgkb	rs367956522
gwascentral	rs367956522
openSNP	rs367956522
23andMe	rs367956522
SNPshot	rs367956522
SNPdbe	rs367956522
MSV3d	rs367956522
GWAS Ctlg	rs367956522

Max Magnitude

0

ClinVar
Risk	rs367956522(C;C)
Alt	rs367956522(C;C)
Reference	Rs367956522(T;T)
Significance	Pathogenic
Disease	Wilson disease not provided
Variation	info
Gene	ATP7B
CLNDBN	Wilson disease not provided
Reversed	0
HGVS	NC_000013.10:g.52523934T>C
CLNSRC
CLNACC	RCV000169025.1, RCV000485754.1,