rs199472865

Orientation

minus

Stabilized

minus

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

Make rs199472865(C;C)

Make rs199472865(C;G)

Reference

GRCh38 38.1/142

Chromosome

7

Position

150959598

Gene

KCNH2

is a	snp
is	mentioned by
dbSNP	rs199472865
dbSNP (classic)	rs199472865
ClinGen	rs199472865
ebi	rs199472865
HLI	rs199472865
Exac	rs199472865
Gnomad	rs199472865
Varsome	rs199472865
LitVar	rs199472865
Map	rs199472865
PheGenI	rs199472865
Biobank	rs199472865
1000 genomes	rs199472865
hgdp	rs199472865
ensembl	rs199472865
geneview	rs199472865
scholar	rs199472865
google	rs199472865
pharmgkb	rs199472865
gwascentral	rs199472865
openSNP	rs199472865
23andMe	rs199472865
SNPshot	rs199472865
SNPdbe	rs199472865
MSV3d	rs199472865
GWAS Ctlg	rs199472865

Max Magnitude

0

ClinVar
Risk	rs199472865(C;C) rs199472865(T;T)
Alt	rs199472865(C;C) rs199472865(T;T)
Reference	Rs199472865(G;G)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNH2
CLNDBN	Congenital long QT syndrome
Reversed	1
HGVS	NC_000007.13:g.150656686C>G
CLNSRC	UniProtKB (protein)
CLNACC	RCV000058235.3,