rs397515405

Orientation

plus

Stabilized

plus

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

Make rs397515405(C;T)

Make rs397515405(T;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

135779411

Gene

KCNT1

is a	snp
is	mentioned by
dbSNP	rs397515405
dbSNP (classic)	rs397515405
ClinGen	rs397515405
ebi	rs397515405
HLI	rs397515405
Exac	rs397515405
Gnomad	rs397515405
Varsome	rs397515405
LitVar	rs397515405
Map	rs397515405
PheGenI	rs397515405
Biobank	rs397515405
1000 genomes	rs397515405
hgdp	rs397515405
ensembl	rs397515405
geneview	rs397515405
scholar	rs397515405
google	rs397515405
pharmgkb	rs397515405
gwascentral	rs397515405
openSNP	rs397515405
23andMe	rs397515405
SNPshot	rs397515405
SNPdbe	rs397515405
MSV3d	rs397515405
GWAS Ctlg	rs397515405

Max Magnitude

0

ClinVar
Risk	rs397515405(T;T)
Alt	rs397515405(T;T)
Reference	Rs397515405(C;C)
Significance	Pathogenic
Disease	Epilepsy
Variation	info
Gene	KCNT1
CLNDBN	Epilepsy, nocturnal frontal lobe, 5
Reversed	0
HGVS	NC_000009.11:g.138671257C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000032797.3,