rs199472896

Orientation

minus

Stabilized

minus

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

Make rs199472896(A;A)

Make rs199472896(A;C)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150952705

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472896
dbSNP (classic)	rs199472896
ClinGen	rs199472896
ebi	rs199472896
HLI	rs199472896
Exac	rs199472896
Gnomad	rs199472896
Varsome	rs199472896
LitVar	rs199472896
Map	rs199472896
PheGenI	rs199472896
Biobank	rs199472896
1000 genomes	rs199472896
hgdp	rs199472896
ensembl	rs199472896
geneview	rs199472896
scholar	rs199472896
google	rs199472896
pharmgkb	rs199472896
gwascentral	rs199472896
openSNP	rs199472896
23andMe	rs199472896
SNPshot	rs199472896
SNPdbe	rs199472896
MSV3d	rs199472896
GWAS Ctlg	rs199472896

Max Magnitude

0

ClinVar
Risk	rs199472896(A;A)
Alt	rs199472896(A;A)
Reference	Rs199472896(C;C)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150649793G>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000057882.3,