rs1060501488

Orientation

plus

Stabilized

plus

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

Make rs1060501488(A;A)

Make rs1060501488(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

22

Position

31778119

Gene

DEPDC5

is a	snp
is	mentioned by
dbSNP	rs1060501488
dbSNP (classic)	rs1060501488
ClinGen	rs1060501488
ebi	rs1060501488
HLI	rs1060501488
Exac	rs1060501488
Gnomad	rs1060501488
Varsome	rs1060501488
LitVar	rs1060501488
Map	rs1060501488
PheGenI	rs1060501488
Biobank	rs1060501488
1000 genomes	rs1060501488
hgdp	rs1060501488
ensembl	rs1060501488
geneview	rs1060501488
scholar	rs1060501488
google	rs1060501488
pharmgkb	rs1060501488
gwascentral	rs1060501488
openSNP	rs1060501488
23andMe	rs1060501488
SNPshot	rs1060501488
SNPdbe	rs1060501488
MSV3d	rs1060501488
GWAS Ctlg	rs1060501488

Max Magnitude

0

ClinVar
Risk	rs1060501488(A;A)
Alt	rs1060501488(A;A)
Reference	Rs1060501488(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.32174105G>A
CLNSRC
CLNACC	RCV000474159.1,