rs148968498

Orientation

plus

Stabilized

plus

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

Make rs148968498(A;A)

Make rs148968498(A;G)

Reference

GRCh38 38.1/142

Chromosome

21

Position

34370558

Gene	KCNE2, LOC105372791

is a	snp
is	mentioned by
dbSNP	rs148968498
dbSNP (classic)	rs148968498
ClinGen	rs148968498
ebi	rs148968498
HLI	rs148968498
Exac	rs148968498
Gnomad	rs148968498
Varsome	rs148968498
LitVar	rs148968498
Map	rs148968498
PheGenI	rs148968498
Biobank	rs148968498
1000 genomes	rs148968498
hgdp	rs148968498
ensembl	rs148968498
geneview	rs148968498
scholar	rs148968498
google	rs148968498
pharmgkb	rs148968498
gwascentral	rs148968498
openSNP	rs148968498
23andMe	rs148968498
SNPshot	rs148968498
SNPdbe	rs148968498
MSV3d	rs148968498
GWAS Ctlg	rs148968498

Max Magnitude

0

ClinVar
Risk	rs148968498(A;A)
Alt	rs148968498(A;A)
Reference	Rs148968498(G;G)
Significance	Untested
Disease	Congenital long QT syndrome Long QT syndrome
Variation	info
Gene	KCNE2
CLNDBN	Congenital long QT syndrome Long QT syndrome
Reversed	0
HGVS	NC_000021.8:g.35742857G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058378.3, RCV000148520.1,