rs1057520235

Orientation

minus

Stabilized

minus

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

Make rs1057520235(C;C)

Make rs1057520235(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

13

Position

51950277

Gene

ATP7B

is a	snp
is	mentioned by
dbSNP	rs1057520235
dbSNP (classic)	rs1057520235
ClinGen	rs1057520235
ebi	rs1057520235
HLI	rs1057520235
Exac	rs1057520235
Gnomad	rs1057520235
Varsome	rs1057520235
LitVar	rs1057520235
Map	rs1057520235
PheGenI	rs1057520235
Biobank	rs1057520235
1000 genomes	rs1057520235
hgdp	rs1057520235
ensembl	rs1057520235
geneview	rs1057520235
scholar	rs1057520235
google	rs1057520235
pharmgkb	rs1057520235
gwascentral	rs1057520235
openSNP	rs1057520235
23andMe	rs1057520235
SNPshot	rs1057520235
SNPdbe	rs1057520235
MSV3d	rs1057520235
GWAS Ctlg	rs1057520235

Max Magnitude

0

ClinVar
Risk	rs1057520235(C;C)
Alt	rs1057520235(C;C)
Reference	Rs1057520235(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	ATP7B
CLNDBN	not provided
Reversed	1
HGVS	NC_000013.10:g.52524413A>G
CLNSRC
CLNACC	RCV000430661.1,