rs876657390

Orientation

minus

Stabilized

minus

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

Make rs876657390(G;T)

Make rs876657390(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

1

Position

110603889

Gene

KCNA2

is a	snp
is	mentioned by
dbSNP	rs876657390
dbSNP (classic)	rs876657390
ClinGen	rs876657390
ebi	rs876657390
HLI	rs876657390
Exac	rs876657390
Gnomad	rs876657390
Varsome	rs876657390
LitVar	rs876657390
Map	rs876657390
PheGenI	rs876657390
Biobank	rs876657390
1000 genomes	rs876657390
hgdp	rs876657390
ensembl	rs876657390
geneview	rs876657390
scholar	rs876657390
google	rs876657390
pharmgkb	rs876657390
gwascentral	rs876657390
openSNP	rs876657390
23andMe	rs876657390
SNPshot	rs876657390
SNPdbe	rs876657390
MSV3d	rs876657390
GWAS Ctlg	rs876657390

Max Magnitude

0

ClinVar
Risk	rs876657390(T;T)
Alt	rs876657390(T;T)
Reference	Rs876657390(G;G)
Significance	Pathogenic
Disease	Epileptic encephalopathy
Variation	info
Gene	KCNA2
CLNDBN	Epileptic encephalopathy, early infantile, 32
Reversed	1
HGVS	NC_000001.10:g.111146511C>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000170513.3,