rs1057516227

Orientation

minus

Stabilized

minus

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

Make rs1057516227(-;-)

Make rs1057516227(-;CA)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

51937354

Gene

ATP7B

is a	snp
is	mentioned by
dbSNP	rs1057516227
dbSNP (classic)	rs1057516227
ClinGen	rs1057516227
ebi	rs1057516227
HLI	rs1057516227
Exac	rs1057516227
Gnomad	rs1057516227
Varsome	rs1057516227
LitVar	rs1057516227
Map	rs1057516227
PheGenI	rs1057516227
Biobank	rs1057516227
1000 genomes	rs1057516227
hgdp	rs1057516227
ensembl	rs1057516227
geneview	rs1057516227
scholar	rs1057516227
google	rs1057516227
pharmgkb	rs1057516227
gwascentral	rs1057516227
openSNP	rs1057516227
23andMe	rs1057516227
SNPshot	rs1057516227
SNPdbe	rs1057516227
MSV3d	rs1057516227
GWAS Ctlg	rs1057516227

Max Magnitude

0

ClinVar
Risk	rs1057516227(-;-)
Alt	rs1057516227(-;-)
Reference	Rs1057516227(CA;CA)
Significance	Probable-Pathogenic
Disease	Wilson disease
Variation	info
Gene	ATP7B
CLNDBN	Wilson disease
Reversed	1
HGVS	NC_000013.10:g.52511490_52511491delTG
CLNSRC
CLNACC	RCV000410818.1,