rs886039530

Orientation

plus

Stabilized

plus

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

Make rs886039530(C;T)

Make rs886039530(T;T)

Reference

GRCh38.p7 38.3/149

Chromosome

1

Position

160130547

Gene

ATP1A2

is a	snp
is	mentioned by
dbSNP	rs886039530
dbSNP (classic)	rs886039530
ClinGen	rs886039530
ebi	rs886039530
HLI	rs886039530
Exac	rs886039530
Gnomad	rs886039530
Varsome	rs886039530
LitVar	rs886039530
Map	rs886039530
PheGenI	rs886039530
Biobank	rs886039530
1000 genomes	rs886039530
hgdp	rs886039530
ensembl	rs886039530
geneview	rs886039530
scholar	rs886039530
google	rs886039530
pharmgkb	rs886039530
gwascentral	rs886039530
openSNP	rs886039530
23andMe	rs886039530
SNPshot	rs886039530
SNPdbe	rs886039530
MSV3d	rs886039530
GWAS Ctlg	rs886039530

Max Magnitude

0

ClinVar
Risk	rs886039530(T;T)
Alt	rs886039530(T;T)
Reference	Rs886039530(C;C)
Significance	Pathogenic
Disease	not provided Epileptic encephalopathy
Variation	info
Gene	ATP1A2
CLNDBN	not provided Epileptic encephalopathy
Reversed	0
HGVS	NC_000001.10:g.160100337C>T
CLNSRC
CLNACC	RCV000255573.1, RCV000417013.1,