rs199473364

Orientation

plus

Stabilized

plus

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

Make rs199473364(C;C)

Make rs199473364(C;G)

Reference

GRCh38 38.1/142

Chromosome

21

Position

34370671

Gene	KCNE2, LOC105372791

is a	snp
is	mentioned by
dbSNP	rs199473364
dbSNP (classic)	rs199473364
ClinGen	rs199473364
ebi	rs199473364
HLI	rs199473364
Exac	rs199473364
Gnomad	rs199473364
Varsome	rs199473364
LitVar	rs199473364
Map	rs199473364
PheGenI	rs199473364
Biobank	rs199473364
1000 genomes	rs199473364
hgdp	rs199473364
ensembl	rs199473364
geneview	rs199473364
scholar	rs199473364
google	rs199473364
pharmgkb	rs199473364
gwascentral	rs199473364
openSNP	rs199473364
23andMe	rs199473364
SNPshot	rs199473364
SNPdbe	rs199473364
MSV3d	rs199473364
GWAS Ctlg	rs199473364

Max Magnitude

0

ClinVar
Risk	rs199473364(A;A) rs199473364(C;C)
Alt	rs199473364(A;A) rs199473364(C;C)
Reference	Rs199473364(G;G)
Significance	Untested
Disease	Congenital long QT syndrome Long QT syndrome 6
Variation	info
Gene	KCNE2
CLNDBN	Congenital long QT syndrome Long QT syndrome 6
Reversed	0
HGVS	NC_000021.8:g.35742970G>A; NC_000021.8:g.35742970G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058364.3, RCV000464363.1, RCV000058365.3, RCV000228047.1,