rs587777907

Orientation

minus

Stabilized

minus

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

Make rs587777907(A;T)

Make rs587777907(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

150958319

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs587777907
dbSNP (classic)	rs587777907
ClinGen	rs587777907
ebi	rs587777907
HLI	rs587777907
Exac	rs587777907
Gnomad	rs587777907
Varsome	rs587777907
LitVar	rs587777907
Map	rs587777907
PheGenI	rs587777907
Biobank	rs587777907
1000 genomes	rs587777907
hgdp	rs587777907
ensembl	rs587777907
geneview	rs587777907
scholar	rs587777907
google	rs587777907
pharmgkb	rs587777907
gwascentral	rs587777907
openSNP	rs587777907
23andMe	rs587777907
SNPshot	rs587777907
SNPdbe	rs587777907
MSV3d	rs587777907
GWAS Ctlg	rs587777907

Max Magnitude

0

ClinVar
Risk	rs587777907(T;T)
Alt	rs587777907(T;T)
Reference	Rs587777907(A;A)
Significance	Pathogenic
Disease	Long QT syndrome 2
Variation	info
Gene	KCNH2
CLNDBN	Long QT syndrome 2
Reversed	1
HGVS	NC_000007.13:g.150655407T>A
CLNSRC
CLNACC	RCV000144957.2,