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rs587777458

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587777458(C;T)
Make rs587777458(T;T)
ReferenceGRCh38 38.1/142
Chromosome22
Position31857548
GeneDEPDC5
is asnp
is mentioned by
dbSNPrs587777458
ebirs587777458
HLIrs587777458
Exacrs587777458
Varsomers587777458
Maprs587777458
PheGenIrs587777458
hapmaprs587777458
1000 genomesrs587777458
hgdprs587777458
ensemblrs587777458
gopubmedrs587777458
geneviewrs587777458
scholarrs587777458
googlers587777458
pharmgkbrs587777458
gwascentralrs587777458
openSNPrs587777458
23andMers587777458
23andMe allrs587777458
SNP Nexus

SNPshotrs587777458
SNPdbers587777458
MSV3drs587777458
GWAS Ctlgrs587777458
Max Magnitude0
ClinVar
Risk rs587777458(T;T)
Alt rs587777458(T;T)
Reference rs587777458(C;C)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene DEPDC5
CLNDBN Epilepsy, familial focal, with variable foci
Reversed 0
HGVS NC_000022.10:g.32253534C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000128400.2,