rs368507376

Orientation

plus

Stabilized

plus

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

Make rs368507376(A;A)

Make rs368507376(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

2587583

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs368507376
dbSNP (classic)	rs368507376
ClinGen	rs368507376
ebi	rs368507376
HLI	rs368507376
Exac	rs368507376
Gnomad	rs368507376
Varsome	rs368507376
LitVar	rs368507376
Map	rs368507376
PheGenI	rs368507376
Biobank	rs368507376
1000 genomes	rs368507376
hgdp	rs368507376
ensembl	rs368507376
geneview	rs368507376
scholar	rs368507376
google	rs368507376
pharmgkb	rs368507376
gwascentral	rs368507376
openSNP	rs368507376
23andMe	rs368507376
SNPshot	rs368507376
SNPdbe	rs368507376
MSV3d	rs368507376
GWAS Ctlg	rs368507376

Max Magnitude

0

ClinVar
Risk	rs368507376(A;A)
Alt	rs368507376(A;A)
Reference	Rs368507376(G;G)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ1
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.2608813G>A
CLNSRC
CLNACC	RCV000182180.1,