rs1057516643

Orientation

minus

Stabilized

minus

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

Make rs1057516643(-;-)

Make rs1057516643(-;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

51949717

Gene

ATP7B

is a	snp
is	mentioned by
dbSNP	rs1057516643
dbSNP (classic)	rs1057516643
ClinGen	rs1057516643
ebi	rs1057516643
HLI	rs1057516643
Exac	rs1057516643
Gnomad	rs1057516643
Varsome	rs1057516643
LitVar	rs1057516643
Map	rs1057516643
PheGenI	rs1057516643
Biobank	rs1057516643
1000 genomes	rs1057516643
hgdp	rs1057516643
ensembl	rs1057516643
geneview	rs1057516643
scholar	rs1057516643
google	rs1057516643
pharmgkb	rs1057516643
gwascentral	rs1057516643
openSNP	rs1057516643
23andMe	rs1057516643
SNPshot	rs1057516643
SNPdbe	rs1057516643
MSV3d	rs1057516643
GWAS Ctlg	rs1057516643

Max Magnitude

0

ClinVar
Risk	rs1057516643(-;-)
Alt	rs1057516643(-;-)
Reference	Rs1057516643(T;T)
Significance	Pathogenic
Disease	Wilson disease not provided
Variation	info
Gene	ATP7B
CLNDBN	Wilson disease not provided
Reversed	1
HGVS	NC_000013.10:g.52523853delA
CLNSRC
CLNACC	RCV000409795.1, RCV000482624.1,