rs199473363

Orientation

plus

Stabilized

plus

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

Make rs199473363(A;A)

Make rs199473363(A;T)

Reference

GRCh38 38.1/142

Chromosome

21

Position

34370537

Gene	KCNE2, LOC105372791

is a	snp
is	mentioned by
dbSNP	rs199473363
dbSNP (classic)	rs199473363
ClinGen	rs199473363
ebi	rs199473363
HLI	rs199473363
Exac	rs199473363
Gnomad	rs199473363
Varsome	rs199473363
LitVar	rs199473363
Map	rs199473363
PheGenI	rs199473363
Biobank	rs199473363
1000 genomes	rs199473363
hgdp	rs199473363
ensembl	rs199473363
geneview	rs199473363
scholar	rs199473363
google	rs199473363
pharmgkb	rs199473363
gwascentral	rs199473363
openSNP	rs199473363
23andMe	rs199473363
SNPshot	rs199473363
SNPdbe	rs199473363
MSV3d	rs199473363
GWAS Ctlg	rs199473363

Max Magnitude

0

ClinVar
Risk	rs199473363(A;A)
Alt	rs199473363(A;A)
Reference	Rs199473363(T;T)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNE2
CLNDBN	Congenital long QT syndrome
Reversed	0
HGVS	NC_000021.8:g.35742836T>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058376.3,