rs1057516561

Orientation

minus

Stabilized

minus

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

Make rs1057516561(-;C)

Make rs1057516561(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

51975045

Gene

ATP7B

is a	snp
is	mentioned by
dbSNP	rs1057516561
dbSNP (classic)	rs1057516561
ClinGen	rs1057516561
ebi	rs1057516561
HLI	rs1057516561
Exac	rs1057516561
Gnomad	rs1057516561
Varsome	rs1057516561
LitVar	rs1057516561
Map	rs1057516561
PheGenI	rs1057516561
Biobank	rs1057516561
1000 genomes	rs1057516561
hgdp	rs1057516561
ensembl	rs1057516561
geneview	rs1057516561
scholar	rs1057516561
google	rs1057516561
pharmgkb	rs1057516561
gwascentral	rs1057516561
openSNP	rs1057516561
23andMe	rs1057516561
SNPshot	rs1057516561
SNPdbe	rs1057516561
MSV3d	rs1057516561
GWAS Ctlg	rs1057516561

Max Magnitude

0

ClinVar
Risk	rs1057516561(C;C)
Alt	rs1057516561(C;C)
Reference	Rs1057516561(-;-)
Significance	Probable-Pathogenic
Disease	Wilson disease
Variation	info
Gene	ATP7B
CLNDBN	Wilson disease
Reversed	1
HGVS	NC_000013.10:g.52549182dupG
CLNSRC
CLNACC	RCV000410969.1,