rs199473003

Orientation

minus

Stabilized

minus

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

Make rs199473003(C;T)

Make rs199473003(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150948945

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473003
dbSNP (classic)	rs199473003
ClinGen	rs199473003
ebi	rs199473003
HLI	rs199473003
Exac	rs199473003
Gnomad	rs199473003
Varsome	rs199473003
LitVar	rs199473003
Map	rs199473003
PheGenI	rs199473003
Biobank	rs199473003
1000 genomes	rs199473003
hgdp	rs199473003
ensembl	rs199473003
geneview	rs199473003
scholar	rs199473003
google	rs199473003
pharmgkb	rs199473003
gwascentral	rs199473003
openSNP	rs199473003
23andMe	rs199473003
SNPshot	rs199473003
SNPdbe	rs199473003
MSV3d	rs199473003
GWAS Ctlg	rs199473003

Max Magnitude

0

ClinVar
Risk	rs199473003(T;T)
Alt	rs199473003(T;T)
Reference	Rs199473003(C;C)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150646033G>A
CLNSRC	ClinVar
CLNACC	RCV000058128.3,