rs199473666

Orientation

minus

Stabilized

minus

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

Make rs199473666(A;C)

Make rs199473666(C;C)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150974798

Gene	KCNH2, LOC107986861

is a	snp
is	mentioned by
dbSNP	rs199473666
dbSNP (classic)	rs199473666
ClinGen	rs199473666
ebi	rs199473666
HLI	rs199473666
Exac	rs199473666
Gnomad	rs199473666
Varsome	rs199473666
LitVar	rs199473666
Map	rs199473666
PheGenI	rs199473666
Biobank	rs199473666
1000 genomes	rs199473666
hgdp	rs199473666
ensembl	rs199473666
geneview	rs199473666
scholar	rs199473666
google	rs199473666
pharmgkb	rs199473666
gwascentral	rs199473666
openSNP	rs199473666
23andMe	rs199473666
SNPshot	rs199473666
SNPdbe	rs199473666
MSV3d	rs199473666
GWAS Ctlg	rs199473666

Max Magnitude

0

ClinVar
Risk	rs199473666(C;C)
Alt	rs199473666(C;C)
Reference	Rs199473666(A;A)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150671886T>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058095.3,