rs199472924

Orientation

minus

Stabilized

minus

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

Make rs199472924(C;C)

Make rs199472924(C;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150951702

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472924
dbSNP (classic)	rs199472924
ClinGen	rs199472924
ebi	rs199472924
HLI	rs199472924
Exac	rs199472924
Gnomad	rs199472924
Varsome	rs199472924
LitVar	rs199472924
Map	rs199472924
PheGenI	rs199472924
Biobank	rs199472924
1000 genomes	rs199472924
hgdp	rs199472924
ensembl	rs199472924
geneview	rs199472924
scholar	rs199472924
google	rs199472924
pharmgkb	rs199472924
gwascentral	rs199472924
openSNP	rs199472924
23andMe	rs199472924
SNPshot	rs199472924
SNPdbe	rs199472924
MSV3d	rs199472924
GWAS Ctlg	rs199472924

Max Magnitude

0

ClinVar
Risk	rs199472924(C;C)
Alt	rs199472924(C;C)
Reference	Rs199472924(T;T)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150648790A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057946.3,