rs587783306

Orientation

minus

Stabilized

minus

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

Make rs587783306(A;A)

Make rs587783306(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

51949661

Gene

ATP7B

is a	snp
is	mentioned by
dbSNP	rs587783306
dbSNP (classic)	rs587783306
ClinGen	rs587783306
ebi	rs587783306
HLI	rs587783306
Exac	rs587783306
Gnomad	rs587783306
Varsome	rs587783306
LitVar	rs587783306
Map	rs587783306
PheGenI	rs587783306
Biobank	rs587783306
1000 genomes	rs587783306
hgdp	rs587783306
ensembl	rs587783306
geneview	rs587783306
scholar	rs587783306
google	rs587783306
pharmgkb	rs587783306
gwascentral	rs587783306
openSNP	rs587783306
23andMe	rs587783306
SNPshot	rs587783306
SNPdbe	rs587783306
MSV3d	rs587783306
GWAS Ctlg	rs587783306

Max Magnitude

0

ClinVar
Risk	rs587783306(A;A)
Alt	rs587783306(A;A)
Reference	Rs587783306(G;G)
Significance	Other
Disease	Wilson disease
Variation	info
Gene	ATP7B
CLNDBN	Wilson disease
Reversed	1
HGVS	NC_000013.10:g.52523797C>T
CLNSRC
CLNACC	RCV000145266.1,