rs199473670

Orientation

minus

Stabilized

minus

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

Make rs199473670(A;A)

Make rs199473670(A;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150947812

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473670
dbSNP (classic)	rs199473670
ClinGen	rs199473670
ebi	rs199473670
HLI	rs199473670
Exac	rs199473670
Gnomad	rs199473670
Varsome	rs199473670
LitVar	rs199473670
Map	rs199473670
PheGenI	rs199473670
Biobank	rs199473670
1000 genomes	rs199473670
hgdp	rs199473670
ensembl	rs199473670
geneview	rs199473670
scholar	rs199473670
google	rs199473670
pharmgkb	rs199473670
gwascentral	rs199473670
openSNP	rs199473670
23andMe	rs199473670
SNPshot	rs199473670
SNPdbe	rs199473670
MSV3d	rs199473670
GWAS Ctlg	rs199473670

Max Magnitude

0

ClinVar
Risk	rs199473670(A;A)
Alt	rs199473670(A;A)
Reference	Rs199473670(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.150644900C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058160.3,