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rs587776975

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587776975(A;A)
Make rs587776975(A;G)
ReferenceGRCh38 38.1/142
Chromosome22
Position31893655
GeneDEPDC5
is asnp
is mentioned by
dbSNPrs587776975
ebirs587776975
HLIrs587776975
Exacrs587776975
Varsomers587776975
Maprs587776975
PheGenIrs587776975
hapmaprs587776975
1000 genomesrs587776975
hgdprs587776975
ensemblrs587776975
gopubmedrs587776975
geneviewrs587776975
scholarrs587776975
googlers587776975
pharmgkbrs587776975
gwascentralrs587776975
openSNPrs587776975
23andMers587776975
23andMe allrs587776975
SNP Nexus

SNPshotrs587776975
SNPdbers587776975
MSV3drs587776975
GWAS Ctlgrs587776975
Max Magnitude0
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
Reversed 0
HGVS NC_000022.10:g.32289641G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000043582.3,