rs199472860

Orientation

minus

Stabilized

minus

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

Make rs199472860(A;T)

Make rs199472860(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150959712

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472860
dbSNP (classic)	rs199472860
ClinGen	rs199472860
ebi	rs199472860
HLI	rs199472860
Exac	rs199472860
Gnomad	rs199472860
Varsome	rs199472860
LitVar	rs199472860
Map	rs199472860
PheGenI	rs199472860
Biobank	rs199472860
1000 genomes	rs199472860
hgdp	rs199472860
ensembl	rs199472860
geneview	rs199472860
scholar	rs199472860
google	rs199472860
pharmgkb	rs199472860
gwascentral	rs199472860
openSNP	rs199472860
23andMe	rs199472860
SNPshot	rs199472860
SNPdbe	rs199472860
MSV3d	rs199472860
GWAS Ctlg	rs199472860

Max Magnitude

0

ClinVar
Risk	rs199472860(T;T)
Alt	rs199472860(T;T)
Reference	Rs199472860(A;A)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150656800T>A
CLNSRC	ClinVar
CLNACC	RCV000058218.3,