rs886041691

Orientation

plus

Stabilized

plus

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

Chromosome

9

Position

135769982

Gene

KCNT1

is a	snp
is	mentioned by
dbSNP	rs886041691
dbSNP (classic)	rs886041691
ClinGen	rs886041691
ebi	rs886041691
HLI	rs886041691
Exac	rs886041691
Gnomad	rs886041691
Varsome	rs886041691
LitVar	rs886041691
Map	rs886041691
PheGenI	rs886041691
Biobank	rs886041691
1000 genomes	rs886041691
hgdp	rs886041691
ensembl	rs886041691
geneview	rs886041691
scholar	rs886041691
google	rs886041691
pharmgkb	rs886041691
gwascentral	rs886041691
openSNP	rs886041691
23andMe	rs886041691
SNPshot	rs886041691
SNPdbe	rs886041691
MSV3d	rs886041691
GWAS Ctlg	rs886041691

Max Magnitude

0

ClinVar
Risk	rs886041691(G;G)
Alt	rs886041691(G;G)
Reference	Rs886041691(A;A)
Significance	Pathogenic
Disease	not provided Malignant migrating partial seizures of infancy
Variation	info
Gene	KCNT1
CLNDBN	not provided Malignant migrating partial seizures of infancy
Reversed	0
HGVS	NC_000009.11:g.138661828A>G
CLNSRC
CLNACC	RCV000289855.1, RCV000417014.1,