rs138498207

Orientation

plus

Stabilized

plus

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

Make rs138498207(A;A)

Make rs138498207(A;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150950195

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs138498207
dbSNP (classic)	rs138498207
ClinGen	rs138498207
ebi	rs138498207
HLI	rs138498207
Exac	rs138498207
Gnomad	rs138498207
Varsome	rs138498207
LitVar	rs138498207
Map	rs138498207
PheGenI	rs138498207
Biobank	rs138498207
1000 genomes	rs138498207
hgdp	rs138498207
ensembl	rs138498207
geneview	rs138498207
scholar	rs138498207
google	rs138498207
pharmgkb	rs138498207
gwascentral	rs138498207
openSNP	rs138498207
23andMe	rs138498207
SNPshot	rs138498207
SNPdbe	rs138498207
MSV3d	rs138498207
GWAS Ctlg	rs138498207

Max Magnitude

0

ClinVar
Risk	rs138498207(A;A)
Alt	rs138498207(A;A)
Reference	Rs138498207(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.150647283G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058113.3, RCV000148535.2, RCV000181852.2,