rs199473426

Orientation

minus

Stabilized

minus

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

Make rs199473426(G;T)

Make rs199473426(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150951648

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473426
dbSNP (classic)	rs199473426
ClinGen	rs199473426
ebi	rs199473426
HLI	rs199473426
Exac	rs199473426
Gnomad	rs199473426
Varsome	rs199473426
LitVar	rs199473426
Map	rs199473426
PheGenI	rs199473426
Biobank	rs199473426
1000 genomes	rs199473426
hgdp	rs199473426
ensembl	rs199473426
geneview	rs199473426
scholar	rs199473426
google	rs199473426
pharmgkb	rs199473426
gwascentral	rs199473426
openSNP	rs199473426
23andMe	rs199473426
SNPshot	rs199473426
SNPdbe	rs199473426
MSV3d	rs199473426
GWAS Ctlg	rs199473426

Max Magnitude

0

ClinVar
Risk	rs199473426(A;A) rs199473426(T;T)
Alt	rs199473426(A;A) rs199473426(T;T)
Reference	Rs199473426(G;G)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150648736C>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057971.3,