rs587776975

Orientation

plus

Stabilized

plus

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

Make rs587776975(A;A)

Make rs587776975(A;G)

Reference

GRCh38 38.1/142

Chromosome

22

Position

31893655

Gene

DEPDC5

is a	snp
is	mentioned by
dbSNP	rs587776975
dbSNP (classic)	rs587776975
ClinGen	rs587776975
ebi	rs587776975
HLI	rs587776975
Exac	rs587776975
Gnomad	rs587776975
Varsome	rs587776975
LitVar	rs587776975
Map	rs587776975
PheGenI	rs587776975
Biobank	rs587776975
1000 genomes	rs587776975
hgdp	rs587776975
ensembl	rs587776975
geneview	rs587776975
scholar	rs587776975
google	rs587776975
pharmgkb	rs587776975
gwascentral	rs587776975
openSNP	rs587776975
23andMe	rs587776975
SNPshot	rs587776975
SNPdbe	rs587776975
MSV3d	rs587776975
GWAS Ctlg	rs587776975

Max Magnitude

0

ClinVar
Risk	rs587776975(A;A)
Alt	rs587776975(A;A)
Reference	Rs587776975(G;G)
Significance	Pathogenic
Disease	Epilepsy
Variation	info
Gene	DEPDC5
CLNDBN	Epilepsy, familial focal, with variable foci 1
Reversed	0
HGVS	NC_000022.10:g.32289641G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000043582.6,