rs199473537

Orientation

minus

Stabilized

minus

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

Make rs199473537(C;C)

Make rs199473537(C;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150948996

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473537
dbSNP (classic)	rs199473537
ClinGen	rs199473537
ebi	rs199473537
HLI	rs199473537
Exac	rs199473537
Gnomad	rs199473537
Varsome	rs199473537
LitVar	rs199473537
Map	rs199473537
PheGenI	rs199473537
Biobank	rs199473537
1000 genomes	rs199473537
hgdp	rs199473537
ensembl	rs199473537
geneview	rs199473537
scholar	rs199473537
google	rs199473537
pharmgkb	rs199473537
gwascentral	rs199473537
openSNP	rs199473537
23andMe	rs199473537
SNPshot	rs199473537
SNPdbe	rs199473537
MSV3d	rs199473537
GWAS Ctlg	rs199473537

Max Magnitude

0

ClinVar
Risk	rs199473537(C;C)
Alt	rs199473537(C;C)
Reference	Rs199473537(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.150646084A>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058122.3,