rs1057516740

Orientation

minus

Stabilized

minus

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

Make rs1057516740(-;-)

Make rs1057516740(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

51937579

Gene

ATP7B

is a	snp
is	mentioned by
dbSNP	rs1057516740
dbSNP (classic)	rs1057516740
ClinGen	rs1057516740
ebi	rs1057516740
HLI	rs1057516740
Exac	rs1057516740
Gnomad	rs1057516740
Varsome	rs1057516740
LitVar	rs1057516740
Map	rs1057516740
PheGenI	rs1057516740
Biobank	rs1057516740
1000 genomes	rs1057516740
hgdp	rs1057516740
ensembl	rs1057516740
geneview	rs1057516740
scholar	rs1057516740
google	rs1057516740
pharmgkb	rs1057516740
gwascentral	rs1057516740
openSNP	rs1057516740
23andMe	rs1057516740
SNPshot	rs1057516740
SNPdbe	rs1057516740
MSV3d	rs1057516740
GWAS Ctlg	rs1057516740

Max Magnitude

0

ClinVar
Risk	rs1057516740(-;-)
Alt	rs1057516740(-;-)
Reference	Rs1057516740(A;A)
Significance	Probable-Pathogenic
Disease	Wilson disease
Variation	info
Gene	ATP7B
CLNDBN	Wilson disease
Reversed	1
HGVS	NC_000013.10:g.52511715delT
CLNSRC
CLNACC	RCV000412326.1,