rs199472901

Orientation

minus

Stabilized

minus

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

Make rs199472901(C;T)

Make rs199472901(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150952675

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472901
dbSNP (classic)	rs199472901
ClinGen	rs199472901
ebi	rs199472901
HLI	rs199472901
Exac	rs199472901
Gnomad	rs199472901
Varsome	rs199472901
LitVar	rs199472901
Map	rs199472901
PheGenI	rs199472901
Biobank	rs199472901
1000 genomes	rs199472901
hgdp	rs199472901
ensembl	rs199472901
geneview	rs199472901
scholar	rs199472901
google	rs199472901
pharmgkb	rs199472901
gwascentral	rs199472901
openSNP	rs199472901
23andMe	rs199472901
SNPshot	rs199472901
SNPdbe	rs199472901
MSV3d	rs199472901
GWAS Ctlg	rs199472901

Max Magnitude

0

ClinVar
Risk	rs199472901(T;T)
Alt	rs199472901(T;T)
Reference	Rs199472901(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.150649763G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057891.3,