rs199473414

Orientation

minus

Stabilized

minus

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

Make rs199473414(C;G)

Make rs199473414(G;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150974826

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs199473414
dbSNP (classic)	rs199473414
ClinGen	rs199473414
ebi	rs199473414
HLI	rs199473414
Exac	rs199473414
Gnomad	rs199473414
Varsome	rs199473414
LitVar	rs199473414
Map	rs199473414
PheGenI	rs199473414
Biobank	rs199473414
1000 genomes	rs199473414
hgdp	rs199473414
ensembl	rs199473414
geneview	rs199473414
scholar	rs199473414
google	rs199473414
pharmgkb	rs199473414
gwascentral	rs199473414
openSNP	rs199473414
23andMe	rs199473414
SNPshot	rs199473414
SNPdbe	rs199473414
MSV3d	rs199473414
GWAS Ctlg	rs199473414

Max Magnitude

0

ClinVar
Risk	rs199473414(G;G)
Alt	rs199473414(G;G)
Reference	Rs199473414(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.150671914G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058057.3,