rs199473668

Orientation

minus

Stabilized

minus

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

Make rs199473668(A;A)

Make rs199473668(A;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150948455

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473668
dbSNP (classic)	rs199473668
ClinGen	rs199473668
ebi	rs199473668
HLI	rs199473668
Exac	rs199473668
Gnomad	rs199473668
Varsome	rs199473668
LitVar	rs199473668
Map	rs199473668
PheGenI	rs199473668
Biobank	rs199473668
1000 genomes	rs199473668
hgdp	rs199473668
ensembl	rs199473668
geneview	rs199473668
scholar	rs199473668
google	rs199473668
pharmgkb	rs199473668
gwascentral	rs199473668
openSNP	rs199473668
23andMe	rs199473668
SNPshot	rs199473668
SNPdbe	rs199473668
MSV3d	rs199473668
GWAS Ctlg	rs199473668

Max Magnitude

0

ClinVar
Risk	rs199473668(A;A) rs199473668(T;T)
Alt	rs199473668(A;A) rs199473668(T;T)
Reference	Rs199473668(G;G)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150645543C>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058150.3,