Have questions? Visit https://www.reddit.com/r/SNPedia

rs564667614

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs564667614(C;T)
Make rs564667614(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position31843170
GeneDEPDC5
is asnp
is mentioned by
dbSNPrs564667614
ebirs564667614
HLIrs564667614
Exacrs564667614
Varsomers564667614
Maprs564667614
PheGenIrs564667614
hapmaprs564667614
1000 genomesrs564667614
hgdprs564667614
ensemblrs564667614
gopubmedrs564667614
geneviewrs564667614
scholarrs564667614
googlers564667614
pharmgkbrs564667614
gwascentralrs564667614
openSNPrs564667614
23andMers564667614
23andMe allrs564667614
SNP Nexus

SNPshotrs564667614
SNPdbers564667614
MSV3drs564667614
GWAS Ctlgrs564667614
Max Magnitude0
ClinVar
Risk rs564667614(T;T)
Alt rs564667614(T;T)
Reference rs564667614(C;C)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene DEPDC5
CLNDBN Epilepsy, familial focal, with variable foci
Reversed 0
HGVS NC_000022.10:g.32239156C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000157607.3,