rs1057523338

Orientation

minus

Stabilized

minus

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

Make rs1057523338(A;G)

Make rs1057523338(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

150951093

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs1057523338
dbSNP (classic)	rs1057523338
ClinGen	rs1057523338
ebi	rs1057523338
HLI	rs1057523338
Exac	rs1057523338
Gnomad	rs1057523338
Varsome	rs1057523338
LitVar	rs1057523338
Map	rs1057523338
PheGenI	rs1057523338
Biobank	rs1057523338
1000 genomes	rs1057523338
hgdp	rs1057523338
ensembl	rs1057523338
geneview	rs1057523338
scholar	rs1057523338
google	rs1057523338
pharmgkb	rs1057523338
gwascentral	rs1057523338
openSNP	rs1057523338
23andMe	rs1057523338
SNPshot	rs1057523338
SNPdbe	rs1057523338
MSV3d	rs1057523338
GWAS Ctlg	rs1057523338

Max Magnitude

0

ClinVar
Risk	rs1057523338(G;G)
Alt	rs1057523338(G;G)
Reference	Rs1057523338(A;A)
Significance	Probable-Pathogenic
Disease	not provided Long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	not provided Long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150648181T>C
CLNSRC
CLNACC	RCV000426599.1, RCV000466780.1,