rs876661350

Orientation

plus

Stabilized

plus

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

Make rs876661350(A;A)

Make rs876661350(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

11

Position

2570678

Gene

KCNQ1

is a	snp
is	mentioned by
dbSNP	rs876661350
dbSNP (classic)	rs876661350
ClinGen	rs876661350
ebi	rs876661350
HLI	rs876661350
Exac	rs876661350
Gnomad	rs876661350
Varsome	rs876661350
LitVar	rs876661350
Map	rs876661350
PheGenI	rs876661350
Biobank	rs876661350
1000 genomes	rs876661350
hgdp	rs876661350
ensembl	rs876661350
geneview	rs876661350
scholar	rs876661350
google	rs876661350
pharmgkb	rs876661350
gwascentral	rs876661350
openSNP	rs876661350
23andMe	rs876661350
SNPshot	rs876661350
SNPdbe	rs876661350
MSV3d	rs876661350
GWAS Ctlg	rs876661350

Max Magnitude

0

ClinVar
Risk	rs876661350(A;A)
Alt	rs876661350(A;A)
Reference	Rs876661350(G;G)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNQ1
CLNDBN	not provided
Reversed	0
HGVS	NC_000011.9:g.2591908G>A
CLNSRC
CLNACC	RCV000223822.1,