rs397515406

Orientation

plus

Stabilized

plus

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

Make rs397515406(C;C)

Make rs397515406(C;T)

Reference

GRCh38 38.1/141

Chromosome

9

Position

135777374

Gene

KCNT1

is a	snp
is	mentioned by
dbSNP	rs397515406
dbSNP (classic)	rs397515406
ClinGen	rs397515406
ebi	rs397515406
HLI	rs397515406
Exac	rs397515406
Gnomad	rs397515406
Varsome	rs397515406
LitVar	rs397515406
Map	rs397515406
PheGenI	rs397515406
Biobank	rs397515406
1000 genomes	rs397515406
hgdp	rs397515406
ensembl	rs397515406
geneview	rs397515406
scholar	rs397515406
google	rs397515406
pharmgkb	rs397515406
gwascentral	rs397515406
openSNP	rs397515406
23andMe	rs397515406
SNPshot	rs397515406
SNPdbe	rs397515406
MSV3d	rs397515406
GWAS Ctlg	rs397515406

Max Magnitude

0

ClinVar
Risk	rs397515406(C;C)
Alt	rs397515406(C;C)
Reference	Rs397515406(T;T)
Significance	Pathogenic
Disease	Epilepsy
Variation	info
Gene	KCNT1
CLNDBN	Epilepsy, nocturnal frontal lobe, 5
Reversed	0
HGVS	NC_000009.11:g.138669220T>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000032798.3,