rs199472908

Orientation

minus

Stabilized

minus

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

Make rs199472908(A;A)

Make rs199472908(A;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150952556

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472908
dbSNP (classic)	rs199472908
ClinGen	rs199472908
ebi	rs199472908
HLI	rs199472908
Exac	rs199472908
Gnomad	rs199472908
Varsome	rs199472908
LitVar	rs199472908
Map	rs199472908
PheGenI	rs199472908
Biobank	rs199472908
1000 genomes	rs199472908
hgdp	rs199472908
ensembl	rs199472908
geneview	rs199472908
scholar	rs199472908
google	rs199472908
pharmgkb	rs199472908
gwascentral	rs199472908
openSNP	rs199472908
23andMe	rs199472908
SNPshot	rs199472908
SNPdbe	rs199472908
MSV3d	rs199472908
GWAS Ctlg	rs199472908

Max Magnitude

0

ClinVar
Risk	rs199472908(A;A)
Alt	rs199472908(A;A)
Reference	Rs199472908(G;G)
Significance	Untested
Disease	Congenital long QT syndrome not specified
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome not specified
Reversed	1
HGVS	NC_000007.13:g.150649644C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057908.3, RCV000454941.1,