rs1057520598

Orientation

minus

Stabilized

minus

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

Make rs1057520598(A;G)

Make rs1057520598(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

150959738

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs1057520598
dbSNP (classic)	rs1057520598
ClinGen	rs1057520598
ebi	rs1057520598
HLI	rs1057520598
Exac	rs1057520598
Gnomad	rs1057520598
Varsome	rs1057520598
LitVar	rs1057520598
Map	rs1057520598
PheGenI	rs1057520598
Biobank	rs1057520598
1000 genomes	rs1057520598
hgdp	rs1057520598
ensembl	rs1057520598
geneview	rs1057520598
scholar	rs1057520598
google	rs1057520598
pharmgkb	rs1057520598
gwascentral	rs1057520598
openSNP	rs1057520598
23andMe	rs1057520598
SNPshot	rs1057520598
SNPdbe	rs1057520598
MSV3d	rs1057520598
GWAS Ctlg	rs1057520598

Max Magnitude

0

ClinVar
Risk	rs1057520598(G;G)
Alt	rs1057520598(G;G)
Reference	Rs1057520598(A;A)
Significance	Pathogenic
Disease	not provided Long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	not provided Long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150656826T>C
CLNSRC
CLNACC	RCV000427208.1, RCV000460573.1,