rs1057518867

Orientation

minus

Stabilized

minus

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

Make rs1057518867(A;A)

Make rs1057518867(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

51946381

Gene

ATP7B

is a	snp
is	mentioned by
dbSNP	rs1057518867
dbSNP (classic)	rs1057518867
ClinGen	rs1057518867
ebi	rs1057518867
HLI	rs1057518867
Exac	rs1057518867
Gnomad	rs1057518867
Varsome	rs1057518867
LitVar	rs1057518867
Map	rs1057518867
PheGenI	rs1057518867
Biobank	rs1057518867
1000 genomes	rs1057518867
hgdp	rs1057518867
ensembl	rs1057518867
geneview	rs1057518867
scholar	rs1057518867
google	rs1057518867
pharmgkb	rs1057518867
gwascentral	rs1057518867
openSNP	rs1057518867
23andMe	rs1057518867
SNPshot	rs1057518867
SNPdbe	rs1057518867
MSV3d	rs1057518867
GWAS Ctlg	rs1057518867

Max Magnitude

0

ClinVar
Risk	rs1057518867(A;A)
Alt	rs1057518867(A;A)
Reference	Rs1057518867(G;G)
Significance	Probable-Pathogenic
Disease	Hand tremor Kayser-Fleischer ring
Variation	info
Gene	ATP7B
CLNDBN	Hand tremor Kayser-Fleischer ring
Reversed	1
HGVS	NC_000013.10:g.52520517C>T
CLNSRC
CLNACC	RCV000415306.1,