rs774588571

Orientation

plus

Stabilized

plus

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

Make rs774588571(C;T)

Make rs774588571(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

9

Position

135770048

Gene

KCNT1

is a	snp
is	mentioned by
dbSNP	rs774588571
dbSNP (classic)	rs774588571
ClinGen	rs774588571
ebi	rs774588571
HLI	rs774588571
Exac	rs774588571
Gnomad	rs774588571
Varsome	rs774588571
LitVar	rs774588571
Map	rs774588571
PheGenI	rs774588571
Biobank	rs774588571
1000 genomes	rs774588571
hgdp	rs774588571
ensembl	rs774588571
geneview	rs774588571
scholar	rs774588571
google	rs774588571
pharmgkb	rs774588571
gwascentral	rs774588571
openSNP	rs774588571
23andMe	rs774588571
SNPshot	rs774588571
SNPdbe	rs774588571
MSV3d	rs774588571
GWAS Ctlg	rs774588571

Max Magnitude

0

ClinVar
Risk	rs774588571(T;T)
Alt	rs774588571(T;T)
Reference	Rs774588571(C;C)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	KCNT1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.138661894C>T
CLNSRC
CLNACC	RCV000429853.1,