rs141423405

Orientation

plus

Stabilized

plus

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

Make rs141423405(C;T)

Make rs141423405(T;T)

Reference

GRCh38 38.1/142

Chromosome

21

Position

34370707

Gene	KCNE2, LOC105372791

is a	snp
is	mentioned by
dbSNP	rs141423405
dbSNP (classic)	rs141423405
ClinGen	rs141423405
ebi	rs141423405
HLI	rs141423405
Exac	rs141423405
Gnomad	rs141423405
Varsome	rs141423405
LitVar	rs141423405
Map	rs141423405
PheGenI	rs141423405
Biobank	rs141423405
1000 genomes	rs141423405
hgdp	rs141423405
ensembl	rs141423405
geneview	rs141423405
scholar	rs141423405
google	rs141423405
pharmgkb	rs141423405
gwascentral	rs141423405
openSNP	rs141423405
23andMe	rs141423405
SNPshot	rs141423405
SNPdbe	rs141423405
MSV3d	rs141423405
GWAS Ctlg	rs141423405

Max Magnitude

0

ClinVar
Risk	rs141423405(T;T)
Alt	rs141423405(T;T)
Reference	Rs141423405(C;C)
Significance	Untested
Disease	Congenital long QT syndrome Long QT syndrome not specified
Variation	info
Gene	KCNE2
CLNDBN	Congenital long QT syndrome Long QT syndrome not specified
Reversed	0
HGVS	NC_000021.8:g.35743006C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058367.3, RCV000148522.1, RCV000170957.4,