rs199473021

Orientation

minus

Stabilized

minus

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

Make rs199473021(C;T)

Make rs199473021(T;T)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150947383

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473021
dbSNP (classic)	rs199473021
ClinGen	rs199473021
ebi	rs199473021
HLI	rs199473021
Exac	rs199473021
Gnomad	rs199473021
Varsome	rs199473021
LitVar	rs199473021
Map	rs199473021
PheGenI	rs199473021
Biobank	rs199473021
1000 genomes	rs199473021
hgdp	rs199473021
ensembl	rs199473021
geneview	rs199473021
scholar	rs199473021
google	rs199473021
pharmgkb	rs199473021
gwascentral	rs199473021
openSNP	rs199473021
23andMe	rs199473021
SNPshot	rs199473021
SNPdbe	rs199473021
MSV3d	rs199473021
GWAS Ctlg	rs199473021

Max Magnitude

0

ClinVar
Risk	rs199473021(A;A) rs199473021(T;T)
Alt	rs199473021(A;A) rs199473021(T;T)
Reference	Rs199473021(C;C)
Significance	Probable-non-pathogenic
Disease	Congenital long QT syndrome not specified
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome not specified
Reversed	1
HGVS	NC_000007.13:g.150644471G>A; NC_000007.13:g.150644471G>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058195.3, RCV000430414.1,