rs199473422

Orientation

minus

Stabilized

minus

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

Make rs199473422(C;T)

Make rs199473422(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150974797

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs199473422
dbSNP (classic)	rs199473422
ClinGen	rs199473422
ebi	rs199473422
HLI	rs199473422
Exac	rs199473422
Gnomad	rs199473422
Varsome	rs199473422
LitVar	rs199473422
Map	rs199473422
PheGenI	rs199473422
Biobank	rs199473422
1000 genomes	rs199473422
hgdp	rs199473422
ensembl	rs199473422
geneview	rs199473422
scholar	rs199473422
google	rs199473422
pharmgkb	rs199473422
gwascentral	rs199473422
openSNP	rs199473422
23andMe	rs199473422
SNPshot	rs199473422
SNPdbe	rs199473422
MSV3d	rs199473422
GWAS Ctlg	rs199473422

Max Magnitude

0

ClinVar
Risk	rs199473422(G;G) rs199473422(T;T)
Alt	rs199473422(G;G) rs199473422(T;T)
Reference	Rs199473422(C;C)
Significance	Pathogenic
Disease	not provided Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	not provided Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150671885G>A; NC_000007.13:g.150671885G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058097.4, RCV000058096.3, RCV000182051.1,