rs794729053

Merged into

rs782091454

Orientation

minus

Stabilized

minus

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

Make rs794729053(C;C)

Make rs794729053(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

41767470

Gene

JUP

is a	snp
is	mentioned by
dbSNP	rs794729053
dbSNP (classic)	rs794729053
ClinGen	rs794729053
ebi	rs794729053
HLI	rs794729053
Exac	rs794729053
Gnomad	rs794729053
Varsome	rs794729053
LitVar	rs794729053
Map	rs794729053
PheGenI	rs794729053
Biobank	rs794729053
1000 genomes	rs794729053
hgdp	rs794729053
ensembl	rs794729053
geneview	rs794729053
scholar	rs794729053
google	rs794729053
pharmgkb	rs794729053
gwascentral	rs794729053
openSNP	rs794729053
23andMe	rs794729053
SNPshot	rs794729053
SNPdbe	rs794729053
MSV3d	rs794729053
GWAS Ctlg	rs794729053

Status

Merged into rs782091454

Max Magnitude

0

ClinVar
Risk	rs794729053(C;C)
Alt	rs794729053(C;C)
Reference	Rs794729053(T;T)
Significance	Probable-Pathogenic
Disease	Cardiac arrhythmia
Variation	info
Gene	JUP
CLNDBN	Cardiac arrhythmia
Reversed	1
HGVS	NC_000017.10:g.39923722A>G
CLNSRC
CLNACC	RCV000183509.1,