rs199473038

Orientation

minus

Stabilized

minus

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

Make rs199473038(G;G)

Make rs199473038(G;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150951697

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473038
dbSNP (classic)	rs199473038
ClinGen	rs199473038
ebi	rs199473038
HLI	rs199473038
Exac	rs199473038
Gnomad	rs199473038
Varsome	rs199473038
LitVar	rs199473038
Map	rs199473038
PheGenI	rs199473038
Biobank	rs199473038
1000 genomes	rs199473038
hgdp	rs199473038
ensembl	rs199473038
geneview	rs199473038
scholar	rs199473038
google	rs199473038
pharmgkb	rs199473038
gwascentral	rs199473038
openSNP	rs199473038
23andMe	rs199473038
SNPshot	rs199473038
SNPdbe	rs199473038
MSV3d	rs199473038
GWAS Ctlg	rs199473038

Max Magnitude

0

ClinVar
Risk	rs199473038(G;G)
Alt	rs199473038(G;G)
Reference	Rs199473038(T;T)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150648785A>C
CLNSRC	ClinVar
CLNACC	RCV000057948.3,