rs866242631

Orientation

plus

Stabilized

plus

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

Make rs866242631(C;T)

Make rs866242631(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

9

Position

135768847

Gene

KCNT1

is a	snp
is	mentioned by
dbSNP	rs866242631
dbSNP (classic)	rs866242631
ClinGen	rs866242631
ebi	rs866242631
HLI	rs866242631
Exac	rs866242631
Gnomad	rs866242631
Varsome	rs866242631
LitVar	rs866242631
Map	rs866242631
PheGenI	rs866242631
Biobank	rs866242631
1000 genomes	rs866242631
hgdp	rs866242631
ensembl	rs866242631
geneview	rs866242631
scholar	rs866242631
google	rs866242631
pharmgkb	rs866242631
gwascentral	rs866242631
openSNP	rs866242631
23andMe	rs866242631
SNPshot	rs866242631
SNPdbe	rs866242631
MSV3d	rs866242631
GWAS Ctlg	rs866242631

Max Magnitude

0

ClinVar
Risk	rs866242631(A;A) rs866242631(T;T)
Alt	rs866242631(A;A) rs866242631(T;T)
Reference	Rs866242631(C;C)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	KCNT1
CLNDBN	not provided
Reversed	0
HGVS	NC_000009.11:g.138660693C>A; NC_000009.11:g.138660693C>T
CLNSRC
CLNACC	RCV000371693.1, RCV000255800.1,