rs397508100

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(CGTC;CGTC)	0	common in clinvar
(TCCG;TCCG)	0	common in clinvar

Make rs397508100(-;-)

Make rs397508100(-;CGTC)

Reference

GRCh38 38.1/141

Chromosome

11

Position

2777025

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs397508100
dbSNP (classic)	rs397508100
ClinGen	rs397508100
ebi	rs397508100
HLI	rs397508100
Exac	rs397508100
Gnomad	rs397508100
Varsome	rs397508100
LitVar	rs397508100
Map	rs397508100
PheGenI	rs397508100
Biobank	rs397508100
1000 genomes	rs397508100
hgdp	rs397508100
ensembl	rs397508100
geneview	rs397508100
scholar	rs397508100
google	rs397508100
pharmgkb	rs397508100
gwascentral	rs397508100
openSNP	rs397508100
23andMe	rs397508100
SNPshot	rs397508100
SNPdbe	rs397508100
MSV3d	rs397508100
GWAS Ctlg	rs397508100

Max Magnitude

0

ClinVar
Risk	rs397508100(-;-)
Alt	rs397508100(-;-)
Reference	Rs397508100(TCCG;TCCG)
Significance	Untested
Disease	Long QT syndrome
Variation	info
Gene	KCNQ1
CLNDBN	Long QT syndrome, LQT1 subtype
Reversed	0
HGVS	NC_000011.9:g.2798255_2798258delCGTC
CLNSRC	ClinVar
CLNACC	RCV000046022.2,