rs886044717

Orientation

plus

Stabilized

plus

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

Chromosome

9

Position

135779423

Gene

KCNT1

is a	snp
is	mentioned by
dbSNP	rs886044717
dbSNP (classic)	rs886044717
ClinGen	rs886044717
ebi	rs886044717
HLI	rs886044717
Exac	rs886044717
Gnomad	rs886044717
Varsome	rs886044717
LitVar	rs886044717
Map	rs886044717
PheGenI	rs886044717
Biobank	rs886044717
1000 genomes	rs886044717
hgdp	rs886044717
ensembl	rs886044717
geneview	rs886044717
scholar	rs886044717
google	rs886044717
pharmgkb	rs886044717
gwascentral	rs886044717
openSNP	rs886044717
23andMe	rs886044717
SNPshot	rs886044717
SNPdbe	rs886044717
MSV3d	rs886044717
GWAS Ctlg	rs886044717

Max Magnitude

0

ClinVar
Risk	rs886044717(A;A)
Alt	rs886044717(A;A)
Reference	Rs886044717(T;T)
Significance	Pathogenic
Disease	Early infantile epileptic encephalopathy 14
Variation	info
Gene	KCNT1
CLNDBN	Early infantile epileptic encephalopathy 14
Reversed	0
HGVS	NC_000009.11:g.138671269T>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000077799.3,