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rs587776977

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776977(C;T)
Make rs587776977(T;T)
ReferenceGRCh38 38.1/142
Chromosome22
Position31802739
GeneDEPDC5
is asnp
is mentioned by
dbSNPrs587776977
ebirs587776977
HLIrs587776977
Exacrs587776977
Varsomers587776977
Maprs587776977
PheGenIrs587776977
hapmaprs587776977
1000 genomesrs587776977
hgdprs587776977
ensemblrs587776977
gopubmedrs587776977
geneviewrs587776977
scholarrs587776977
googlers587776977
pharmgkbrs587776977
gwascentralrs587776977
openSNPrs587776977
23andMers587776977
23andMe allrs587776977
SNP Nexus

SNPshotrs587776977
SNPdbers587776977
MSV3drs587776977
GWAS Ctlgrs587776977
Max Magnitude0
ClinVar
Risk rs587776977(T;T)
Alt rs587776977(T;T)
Reference rs587776977(C;C)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene DEPDC5
CLNDBN Epilepsy, familial focal, with variable foci
Reversed 0
HGVS NC_000022.10:g.32198725C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000043585.2,