rs886039397

Orientation

plus

Stabilized

plus

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

Make rs886039397(C;C)

Make rs886039397(C;T)

Reference

GRCh38.p7 38.3/149

Chromosome

9

Position

135768853

Gene

KCNT1

is a	snp
is	mentioned by
dbSNP	rs886039397
dbSNP (classic)	rs886039397
ClinGen	rs886039397
ebi	rs886039397
HLI	rs886039397
Exac	rs886039397
Gnomad	rs886039397
Varsome	rs886039397
LitVar	rs886039397
Map	rs886039397
PheGenI	rs886039397
Biobank	rs886039397
1000 genomes	rs886039397
hgdp	rs886039397
ensembl	rs886039397
geneview	rs886039397
scholar	rs886039397
google	rs886039397
pharmgkb	rs886039397
gwascentral	rs886039397
openSNP	rs886039397
23andMe	rs886039397
SNPshot	rs886039397
SNPdbe	rs886039397
MSV3d	rs886039397
GWAS Ctlg	rs886039397

Max Magnitude

0

ClinVar
Risk	rs886039397(C;C)
Alt	rs886039397(C;C)
Reference	Rs886039397(T;T)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNT1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.138660699T>C
CLNSRC
CLNACC	RCV000254881.1,