rs149955375

Orientation

plus

Stabilized

plus

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

Make rs149955375(A;A)

Make rs149955375(A;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150947623

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs149955375
dbSNP (classic)	rs149955375
ClinGen	rs149955375
ebi	rs149955375
HLI	rs149955375
Exac	rs149955375
Gnomad	rs149955375
Varsome	rs149955375
LitVar	rs149955375
Map	rs149955375
PheGenI	rs149955375
Biobank	rs149955375
1000 genomes	rs149955375
hgdp	rs149955375
ensembl	rs149955375
geneview	rs149955375
scholar	rs149955375
google	rs149955375
pharmgkb	rs149955375
gwascentral	rs149955375
openSNP	rs149955375
23andMe	rs149955375
SNPshot	rs149955375
SNPdbe	rs149955375
MSV3d	rs149955375
GWAS Ctlg	rs149955375

Max Magnitude

0

ClinVar
Risk	rs149955375(A;A)
Alt	rs149955375(A;A)
Reference	Rs149955375(G;G)
Significance	Other
Disease	Congenital long QT syndrome Long QT syndrome not specified
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome Long QT syndrome not specified
Reversed	0
HGVS	NC_000007.13:g.150644711G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058182.3, RCV000148532.4, RCV000181901.5,