rs199472936

Orientation

minus

Stabilized

minus

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

Make rs199472936(G;T)

Make rs199472936(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150951592

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472936
dbSNP (classic)	rs199472936
ClinGen	rs199472936
ebi	rs199472936
HLI	rs199472936
Exac	rs199472936
Gnomad	rs199472936
Varsome	rs199472936
LitVar	rs199472936
Map	rs199472936
PheGenI	rs199472936
Biobank	rs199472936
1000 genomes	rs199472936
hgdp	rs199472936
ensembl	rs199472936
geneview	rs199472936
scholar	rs199472936
google	rs199472936
pharmgkb	rs199472936
gwascentral	rs199472936
openSNP	rs199472936
23andMe	rs199472936
SNPshot	rs199472936
SNPdbe	rs199472936
MSV3d	rs199472936
GWAS Ctlg	rs199472936

Max Magnitude

0

ClinVar
Risk	rs199472936(A;A) rs199472936(T;T)
Alt	rs199472936(A;A) rs199472936(T;T)
Reference	Rs199472936(G;G)
Significance	Pathogenic
Disease	Congenital long QT syndrome Long QT syndrome 2 Long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome Long QT syndrome 2 Long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150648680C>A; NC_000007.13:g.150648680C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057996.3, RCV000057995.3, RCV000208241.1, RCV000233419.1,