rs199473029

Orientation

minus

Stabilized

minus

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

Make rs199473029(A;G)

Make rs199473029(G;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150946974

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199473029
dbSNP (classic)	rs199473029
ClinGen	rs199473029
ebi	rs199473029
HLI	rs199473029
Exac	rs199473029
Gnomad	rs199473029
Varsome	rs199473029
LitVar	rs199473029
Map	rs199473029
PheGenI	rs199473029
Biobank	rs199473029
1000 genomes	rs199473029
hgdp	rs199473029
ensembl	rs199473029
geneview	rs199473029
scholar	rs199473029
google	rs199473029
pharmgkb	rs199473029
gwascentral	rs199473029
openSNP	rs199473029
23andMe	rs199473029
SNPshot	rs199473029
SNPdbe	rs199473029
MSV3d	rs199473029
GWAS Ctlg	rs199473029

Max Magnitude

0

ClinVar
Risk	rs199473029(G;G)
Alt	rs199473029(G;G)
Reference	Rs199473029(A;A)
Significance	Untested
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.150644062T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058212.3, RCV000455396.1,