rs1057516479

Orientation

minus

Stabilized

minus

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

Make rs1057516479(C;T)

Make rs1057516479(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

51941108

Gene

ATP7B

is a	snp
is	mentioned by
dbSNP	rs1057516479
dbSNP (classic)	rs1057516479
ClinGen	rs1057516479
ebi	rs1057516479
HLI	rs1057516479
Exac	rs1057516479
Gnomad	rs1057516479
Varsome	rs1057516479
LitVar	rs1057516479
Map	rs1057516479
PheGenI	rs1057516479
Biobank	rs1057516479
1000 genomes	rs1057516479
hgdp	rs1057516479
ensembl	rs1057516479
geneview	rs1057516479
scholar	rs1057516479
google	rs1057516479
pharmgkb	rs1057516479
gwascentral	rs1057516479
openSNP	rs1057516479
23andMe	rs1057516479
SNPshot	rs1057516479
SNPdbe	rs1057516479
MSV3d	rs1057516479
GWAS Ctlg	rs1057516479

Max Magnitude

0

ClinVar
Risk	rs1057516479(T;T)
Alt	rs1057516479(T;T)
Reference	Rs1057516479(C;C)
Significance	Probable-Pathogenic
Disease	Wilson disease
Variation	info
Gene	ATP7B
CLNDBN	Wilson disease
Reversed	1
HGVS	NC_000013.10:g.52515244G>A
CLNSRC
CLNACC	RCV000412086.1,