rs199472984

Orientation

minus

Stabilized

minus

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

Make rs199472984(C;T)

Make rs199472984(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150950980

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472984
dbSNP (classic)	rs199472984
ClinGen	rs199472984
ebi	rs199472984
HLI	rs199472984
Exac	rs199472984
Gnomad	rs199472984
Varsome	rs199472984
LitVar	rs199472984
Map	rs199472984
PheGenI	rs199472984
Biobank	rs199472984
1000 genomes	rs199472984
hgdp	rs199472984
ensembl	rs199472984
geneview	rs199472984
scholar	rs199472984
google	rs199472984
pharmgkb	rs199472984
gwascentral	rs199472984
openSNP	rs199472984
23andMe	rs199472984
SNPshot	rs199472984
SNPdbe	rs199472984
MSV3d	rs199472984
GWAS Ctlg	rs199472984

Max Magnitude

0

ClinVar
Risk	rs199472984(T;T)
Alt	rs199472984(T;T)
Reference	Rs199472984(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.150648068G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058080.3,