rs797044544

Orientation

plus

Stabilized

plus

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

Make rs797044544(A;A)

Make rs797044544(A;G)

Reference

GRCh38.p2 38.2/146

Chromosome

9

Position

135778781

Gene

KCNT1

is a	snp
is	mentioned by
dbSNP	rs797044544
dbSNP (classic)	rs797044544
ClinGen	rs797044544
ebi	rs797044544
HLI	rs797044544
Exac	rs797044544
Gnomad	rs797044544
Varsome	rs797044544
LitVar	rs797044544
Map	rs797044544
PheGenI	rs797044544
Biobank	rs797044544
1000 genomes	rs797044544
hgdp	rs797044544
ensembl	rs797044544
geneview	rs797044544
scholar	rs797044544
google	rs797044544
pharmgkb	rs797044544
gwascentral	rs797044544
openSNP	rs797044544
23andMe	rs797044544
SNPshot	rs797044544
SNPdbe	rs797044544
MSV3d	rs797044544
GWAS Ctlg	rs797044544

Max Magnitude

0

ClinVar
Risk	rs797044544(A;A) rs797044544(C;C)
Alt	rs797044544(A;A) rs797044544(C;C)
Reference	Rs797044544(G;G)
Significance	Pathogenic
Disease	Epilepsy not provided
Variation	info
Gene	KCNT1
CLNDBN	Epilepsy, nocturnal frontal lobe, 5 not provided
Reversed	0
HGVS	NC_000009.11:g.138670627G>A; NC_000009.11:g.138670627G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000192060.2, RCV000425537.1,