rs199472900

Orientation

minus

Stabilized

minus

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

Make rs199472900(A;A)

Make rs199472900(A;C)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150952689

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472900
dbSNP (classic)	rs199472900
ClinGen	rs199472900
ebi	rs199472900
HLI	rs199472900
Exac	rs199472900
Gnomad	rs199472900
Varsome	rs199472900
LitVar	rs199472900
Map	rs199472900
PheGenI	rs199472900
Biobank	rs199472900
1000 genomes	rs199472900
hgdp	rs199472900
ensembl	rs199472900
geneview	rs199472900
scholar	rs199472900
google	rs199472900
pharmgkb	rs199472900
gwascentral	rs199472900
openSNP	rs199472900
23andMe	rs199472900
SNPshot	rs199472900
SNPdbe	rs199472900
MSV3d	rs199472900
GWAS Ctlg	rs199472900

Max Magnitude

0

ClinVar
Risk	rs199472900(A;A)
Alt	rs199472900(A;A)
Reference	Rs199472900(C;C)
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.150649777G>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057890.3, RCV000481749.1,