rs199472881

Orientation

minus

Stabilized

minus

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

Make rs199472881(C;C)

Make rs199472881(C;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150958103

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472881
dbSNP (classic)	rs199472881
ClinGen	rs199472881
ebi	rs199472881
HLI	rs199472881
Exac	rs199472881
Gnomad	rs199472881
Varsome	rs199472881
LitVar	rs199472881
Map	rs199472881
PheGenI	rs199472881
Biobank	rs199472881
1000 genomes	rs199472881
hgdp	rs199472881
ensembl	rs199472881
geneview	rs199472881
scholar	rs199472881
google	rs199472881
pharmgkb	rs199472881
gwascentral	rs199472881
openSNP	rs199472881
23andMe	rs199472881
SNPshot	rs199472881
SNPdbe	rs199472881
MSV3d	rs199472881
GWAS Ctlg	rs199472881

Max Magnitude

0

ClinVar
Risk	rs199472881(C;C) rs199472881(G;G)
Alt	rs199472881(C;C) rs199472881(G;G)
Reference	Rs199472881(T;T)
Significance	Untested
Disease	Long QT syndrome 2 Short QT syndrome 1 Long QT syndrome Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Long QT syndrome 2 Short QT syndrome 1 Long QT syndrome Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150655191A>C; NC_000007.13:g.150655191A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000415641.1, RCV000415675.1, RCV000463158.1, RCV000058266.3,