rs886039373

Orientation

plus

Stabilized

plus

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

Make rs886039373(A;A)

Make rs886039373(A;G)

Reference

GRCh38.p7 38.3/149

Chromosome

5

Position

161882639

Gene

GABRA1

is a	snp
is	mentioned by
dbSNP	rs886039373
dbSNP (classic)	rs886039373
ClinGen	rs886039373
ebi	rs886039373
HLI	rs886039373
Exac	rs886039373
Gnomad	rs886039373
Varsome	rs886039373
LitVar	rs886039373
Map	rs886039373
PheGenI	rs886039373
Biobank	rs886039373
1000 genomes	rs886039373
hgdp	rs886039373
ensembl	rs886039373
geneview	rs886039373
scholar	rs886039373
google	rs886039373
pharmgkb	rs886039373
gwascentral	rs886039373
openSNP	rs886039373
23andMe	rs886039373
SNPshot	rs886039373
SNPdbe	rs886039373
MSV3d	rs886039373
GWAS Ctlg	rs886039373

Max Magnitude

0

ClinVar
Risk	rs886039373(A;A)
Alt	rs886039373(A;A)
Reference	Rs886039373(G;G)
Significance	Pathogenic
Disease	not provided Epileptic encephalopathy
Variation	info
Gene	GABRA1
CLNDBN	not provided Epileptic encephalopathy, early infantile, 19
Reversed	0
HGVS	NC_000005.9:g.161309645G>A
CLNSRC
CLNACC	RCV000254956.1, RCV000417089.2,