rs186924074

Orientation

plus

Stabilized

plus

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

Make rs186924074(A;G)

Make rs186924074(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

51961861

Gene

ATP7B

is a	snp
is	mentioned by
dbSNP	rs186924074
dbSNP (classic)	rs186924074
ClinGen	rs186924074
ebi	rs186924074
HLI	rs186924074
Exac	rs186924074
Gnomad	rs186924074
Varsome	rs186924074
LitVar	rs186924074
Map	rs186924074
PheGenI	rs186924074
Biobank	rs186924074
1000 genomes	rs186924074
hgdp	rs186924074
ensembl	rs186924074
geneview	rs186924074
scholar	rs186924074
google	rs186924074
pharmgkb	rs186924074
gwascentral	rs186924074
openSNP	rs186924074
23andMe	rs186924074
SNPshot	rs186924074
SNPdbe	rs186924074
MSV3d	rs186924074
GWAS Ctlg	rs186924074

Max Magnitude

0

ClinVar
Risk	rs186924074(G;G)
Alt	rs186924074(G;G)
Reference	Rs186924074(A;A)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ATP7B
CLNDBN	not provided
Reversed	0
HGVS	NC_000013.10:g.52535997A>G
CLNSRC
CLNACC	RCV000480322.1,