rs199473367

Orientation

plus

Stabilized

plus

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

Make rs199473367(C;T)

Make rs199473367(T;T)

Reference

GRCh38 38.1/142

Chromosome

21

Position

34370825

Gene	KCNE2, LOC105372791

is a	snp
is	mentioned by
dbSNP	rs199473367
dbSNP (classic)	rs199473367
ClinGen	rs199473367
ebi	rs199473367
HLI	rs199473367
Exac	rs199473367
Gnomad	rs199473367
Varsome	rs199473367
LitVar	rs199473367
Map	rs199473367
PheGenI	rs199473367
Biobank	rs199473367
1000 genomes	rs199473367
hgdp	rs199473367
ensembl	rs199473367
geneview	rs199473367
scholar	rs199473367
google	rs199473367
pharmgkb	rs199473367
gwascentral	rs199473367
openSNP	rs199473367
23andMe	rs199473367
SNPshot	rs199473367
SNPdbe	rs199473367
MSV3d	rs199473367
GWAS Ctlg	rs199473367

Max Magnitude

0

ClinVar
Risk	rs199473367(T;T)
Alt	rs199473367(T;T)
Reference	Rs199473367(C;C)
Significance	Probable-Pathogenic
Disease	Acquired long QT syndrome not provided
Variation	info
Gene	KCNE2
CLNDBN	Acquired long QT syndrome not provided
Reversed	0
HGVS	NC_000021.8:g.35743124C>T
CLNSRC	ClinVar
CLNACC	RCV000058374.3, RCV000222131.2,