rs199472976

Orientation

minus

Stabilized

minus

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

Make rs199472976(C;T)

Make rs199472976(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150951120

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472976
dbSNP (classic)	rs199472976
ClinGen	rs199472976
ebi	rs199472976
HLI	rs199472976
Exac	rs199472976
Gnomad	rs199472976
Varsome	rs199472976
LitVar	rs199472976
Map	rs199472976
PheGenI	rs199472976
Biobank	rs199472976
1000 genomes	rs199472976
hgdp	rs199472976
ensembl	rs199472976
geneview	rs199472976
scholar	rs199472976
google	rs199472976
pharmgkb	rs199472976
gwascentral	rs199472976
openSNP	rs199472976
23andMe	rs199472976
SNPshot	rs199472976
SNPdbe	rs199472976
MSV3d	rs199472976
GWAS Ctlg	rs199472976

Max Magnitude

0

ClinVar
Risk	rs199472976(T;T)
Alt	rs199472976(T;T)
Reference	Rs199472976(C;C)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150648208G>A
CLNSRC	ClinVar
CLNACC	RCV000058066.3,