rs753962912

Orientation

plus

Stabilized

plus

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

Make rs753962912(-;-)

Make rs753962912(-;TA)

Reference

GRCh38.p2 38.2/144

Chromosome

13

Position

51964995

Gene

ATP7B

is a	snp
is	mentioned by
dbSNP	rs753962912
dbSNP (classic)	rs753962912
ClinGen	rs753962912
ebi	rs753962912
HLI	rs753962912
Exac	rs753962912
Gnomad	rs753962912
Varsome	rs753962912
LitVar	rs753962912
Map	rs753962912
PheGenI	rs753962912
Biobank	rs753962912
1000 genomes	rs753962912
hgdp	rs753962912
ensembl	rs753962912
geneview	rs753962912
scholar	rs753962912
google	rs753962912
pharmgkb	rs753962912
gwascentral	rs753962912
openSNP	rs753962912
23andMe	rs753962912
SNPshot	rs753962912
SNPdbe	rs753962912
MSV3d	rs753962912
GWAS Ctlg	rs753962912

Max Magnitude

0

ClinVar
Risk	rs753962912(-;-)
Alt	rs753962912(-;-)
Reference	Rs753962912(TA;TA)
Significance	Other
Disease	Wilson disease
Variation	info
Gene	ATP7B
CLNDBN	Wilson disease
Reversed	0
HGVS	NC_000013.10:g.52539131_52539132delTA
CLNSRC
CLNACC	RCV000169524.2,