rs199472837

Orientation

minus

Stabilized

minus

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

Make rs199472837(G;G)

Make rs199472837(G;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150974891

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs199472837
dbSNP (classic)	rs199472837
ClinGen	rs199472837
ebi	rs199472837
HLI	rs199472837
Exac	rs199472837
Gnomad	rs199472837
Varsome	rs199472837
LitVar	rs199472837
Map	rs199472837
PheGenI	rs199472837
Biobank	rs199472837
1000 genomes	rs199472837
hgdp	rs199472837
ensembl	rs199472837
geneview	rs199472837
scholar	rs199472837
google	rs199472837
pharmgkb	rs199472837
gwascentral	rs199472837
openSNP	rs199472837
23andMe	rs199472837
SNPshot	rs199472837
SNPdbe	rs199472837
MSV3d	rs199472837
GWAS Ctlg	rs199472837

Max Magnitude

0

ClinVar
Risk	rs199472837(G;G)
Alt	rs199472837(G;G)
Reference	Rs199472837(T;T)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150671979A>C
CLNSRC	ClinVar
CLNACC	RCV000057884.3,