rs199473027

Orientation

minus

Stabilized

minus

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

Make rs199473027(C;G)

Make rs199473027(G;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150947011

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473027
dbSNP (classic)	rs199473027
ClinGen	rs199473027
ebi	rs199473027
HLI	rs199473027
Exac	rs199473027
Gnomad	rs199473027
Varsome	rs199473027
LitVar	rs199473027
Map	rs199473027
PheGenI	rs199473027
Biobank	rs199473027
1000 genomes	rs199473027
hgdp	rs199473027
ensembl	rs199473027
geneview	rs199473027
scholar	rs199473027
google	rs199473027
pharmgkb	rs199473027
gwascentral	rs199473027
openSNP	rs199473027
23andMe	rs199473027
SNPshot	rs199473027
SNPdbe	rs199473027
MSV3d	rs199473027
GWAS Ctlg	rs199473027

Max Magnitude

0

ClinVar
Risk	rs199473027(G;G)
Alt	rs199473027(G;G)
Reference	Rs199473027(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.150644099G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058208.3,