rs377095107

Orientation

plus

Stabilized

plus

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

Make rs377095107(A;A)

Make rs377095107(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

7

Position

150947341

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs377095107
dbSNP (classic)	rs377095107
ClinGen	rs377095107
ebi	rs377095107
HLI	rs377095107
Exac	rs377095107
Gnomad	rs377095107
Varsome	rs377095107
LitVar	rs377095107
Map	rs377095107
PheGenI	rs377095107
Biobank	rs377095107
1000 genomes	rs377095107
hgdp	rs377095107
ensembl	rs377095107
geneview	rs377095107
scholar	rs377095107
google	rs377095107
pharmgkb	rs377095107
gwascentral	rs377095107
openSNP	rs377095107
23andMe	rs377095107
SNPshot	rs377095107
SNPdbe	rs377095107
MSV3d	rs377095107
GWAS Ctlg	rs377095107

Max Magnitude

0

ClinVar
Risk	rs377095107(A;A)
Alt	rs377095107(A;A)
Reference	Rs377095107(G;G)
Significance	Probable-Pathogenic
Disease	Long QT syndrome not specified
Variation	info
Gene	KCNH2
CLNDBN	Long QT syndrome not specified
Reversed	0
HGVS	NC_000007.13:g.150644429G>A
CLNSRC
CLNACC	RCV000148531.1, RCV000181913.2,