rs397515403

Orientation

plus

Stabilized

plus

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

Make rs397515403(A;A)

Make rs397515403(A;G)

Reference

GRCh38 38.1/141

Chromosome

9

Position

135779429

Gene

KCNT1

is a	snp
is	mentioned by
dbSNP	rs397515403
dbSNP (classic)	rs397515403
ClinGen	rs397515403
ebi	rs397515403
HLI	rs397515403
Exac	rs397515403
Gnomad	rs397515403
Varsome	rs397515403
LitVar	rs397515403
Map	rs397515403
PheGenI	rs397515403
Biobank	rs397515403
1000 genomes	rs397515403
hgdp	rs397515403
ensembl	rs397515403
geneview	rs397515403
scholar	rs397515403
google	rs397515403
pharmgkb	rs397515403
gwascentral	rs397515403
openSNP	rs397515403
23andMe	rs397515403
SNPshot	rs397515403
SNPdbe	rs397515403
MSV3d	rs397515403
GWAS Ctlg	rs397515403

Max Magnitude

0

ClinVar
Risk	rs397515403(A;A)
Alt	rs397515403(A;A)
Reference	Rs397515403(G;G)
Significance	Pathogenic
Disease	Early infantile epileptic encephalopathy 14 not provided
Variation	info
Gene	KCNT1
CLNDBN	Early infantile epileptic encephalopathy 14 not provided
Reversed	0
HGVS	NC_000009.11:g.138671275G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000032794.4, RCV000494477.1,