rs397515407

Orientation

plus

Stabilized

plus

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

Make rs397515407(A;A)

Make rs397515407(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

135765188

Gene

KCNT1

is a	snp
is	mentioned by
dbSNP	rs397515407
dbSNP (classic)	rs397515407
ClinGen	rs397515407
ebi	rs397515407
HLI	rs397515407
Exac	rs397515407
Gnomad	rs397515407
Varsome	rs397515407
LitVar	rs397515407
Map	rs397515407
PheGenI	rs397515407
Biobank	rs397515407
1000 genomes	rs397515407
hgdp	rs397515407
ensembl	rs397515407
geneview	rs397515407
scholar	rs397515407
google	rs397515407
pharmgkb	rs397515407
gwascentral	rs397515407
openSNP	rs397515407
23andMe	rs397515407
SNPshot	rs397515407
SNPdbe	rs397515407
MSV3d	rs397515407
GWAS Ctlg	rs397515407

Max Magnitude

0

ClinVar
Risk	rs397515407(A;A)
Alt	rs397515407(A;A)
Reference	Rs397515407(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.138657034G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000032799.3, RCV000412976.1,