rs199472787

Orientation

plus

Stabilized

plus

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

Make rs199472787(C;T)

Make rs199472787(T;T)

Reference

GRCh38 38.1/142

Chromosome

11

Position

2768884

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs199472787
dbSNP (classic)	rs199472787
ClinGen	rs199472787
ebi	rs199472787
HLI	rs199472787
Exac	rs199472787
Gnomad	rs199472787
Varsome	rs199472787
LitVar	rs199472787
Map	rs199472787
PheGenI	rs199472787
Biobank	rs199472787
1000 genomes	rs199472787
hgdp	rs199472787
ensembl	rs199472787
geneview	rs199472787
scholar	rs199472787
google	rs199472787
pharmgkb	rs199472787
gwascentral	rs199472787
openSNP	rs199472787
23andMe	rs199472787
SNPshot	rs199472787
SNPdbe	rs199472787
MSV3d	rs199472787
GWAS Ctlg	rs199472787

Max Magnitude

0

ClinVar
Risk	rs199472787(T;T)
Alt	rs199472787(T;T)
Reference	Rs199472787(C;C)
Significance	Untested
Disease	Congenital long QT syndrome not specified
Variation	info
Gene	KCNQ1
CLNDBN	Congenital long QT syndrome not specified
Reversed	0
HGVS	NC_000011.9:g.2790114C>T
CLNSRC	ClinVar
CLNACC	RCV000057595.3, RCV000454758.1,