rs199472769

Orientation

plus

Stabilized

plus

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

Make rs199472769(C;C)

Make rs199472769(C;G)

Reference

GRCh38 38.1/142

Chromosome

11

Position

2587577

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs199472769
dbSNP (classic)	rs199472769
ClinGen	rs199472769
ebi	rs199472769
HLI	rs199472769
Exac	rs199472769
Gnomad	rs199472769
Varsome	rs199472769
LitVar	rs199472769
Map	rs199472769
PheGenI	rs199472769
Biobank	rs199472769
1000 genomes	rs199472769
hgdp	rs199472769
ensembl	rs199472769
geneview	rs199472769
scholar	rs199472769
google	rs199472769
pharmgkb	rs199472769
gwascentral	rs199472769
openSNP	rs199472769
23andMe	rs199472769
SNPshot	rs199472769
SNPdbe	rs199472769
MSV3d	rs199472769
GWAS Ctlg	rs199472769

Max Magnitude

0

ClinVar
Risk	rs199472769(C;C)
Alt	rs199472769(C;C)
Reference	Rs199472769(G;G)
Significance	Untested
Disease	Congenital long QT syndrome
Variation	info
Gene	KCNQ1
CLNDBN	Congenital long QT syndrome
Reversed	0
HGVS	NC_000011.9:g.2608807G>C
CLNSRC	ClinVar
CLNACC	RCV000057561.3,