rs1057517384

Orientation

minus

Stabilized

minus

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

Make rs1057517384(-;GC)

Make rs1057517384(GC;GC)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

51974830

Gene

ATP7B

is a	snp
is	mentioned by
dbSNP	rs1057517384
dbSNP (classic)	rs1057517384
ClinGen	rs1057517384
ebi	rs1057517384
HLI	rs1057517384
Exac	rs1057517384
Gnomad	rs1057517384
Varsome	rs1057517384
LitVar	rs1057517384
Map	rs1057517384
PheGenI	rs1057517384
Biobank	rs1057517384
1000 genomes	rs1057517384
hgdp	rs1057517384
ensembl	rs1057517384
geneview	rs1057517384
scholar	rs1057517384
google	rs1057517384
pharmgkb	rs1057517384
gwascentral	rs1057517384
openSNP	rs1057517384
23andMe	rs1057517384
SNPshot	rs1057517384
SNPdbe	rs1057517384
MSV3d	rs1057517384
GWAS Ctlg	rs1057517384

Max Magnitude

0

ClinVar
Risk	rs1057517384(GC;GC)
Alt	rs1057517384(GC;GC)
Reference	Rs1057517384(-;-)
Significance	Pathogenic
Disease	Wilson disease not provided
Variation	info
Gene	ATP7B
CLNDBN	Wilson disease not provided
Reversed	1
HGVS	NC_000013.10:g.52548967_52548968dupGC
CLNSRC
CLNACC	RCV000409526.1, RCV000489522.1,