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

rs587776974

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TGT;TGT) 0 common in clinvar
Make rs587776974(-;-)
Make rs587776974(-;GTT)
Make rs587776974(GTT;GTT)
ReferenceGRCh38 38.1/142
Chromosome22
Position31783912
GeneDEPDC5
is asnp
is mentioned by
dbSNPrs587776974
ebirs587776974
HLIrs587776974
Exacrs587776974
Varsomers587776974
Maprs587776974
PheGenIrs587776974
hapmaprs587776974
1000 genomesrs587776974
hgdprs587776974
ensemblrs587776974
gopubmedrs587776974
geneviewrs587776974
scholarrs587776974
googlers587776974
pharmgkbrs587776974
gwascentralrs587776974
openSNPrs587776974
23andMers587776974
23andMe allrs587776974
SNP Nexus

SNPshotrs587776974
SNPdbers587776974
MSV3drs587776974
GWAS Ctlgrs587776974
Max Magnitude0
ClinVar
Risk rs587776974(;)
Alt rs587776974(;)
Reference rs587776974(TGT;TGT)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene DEPDC5
CLNDBN Epilepsy, familial focal, with variable foci
Reversed 0
HGVS NC_000022.10:g.32179898_32179900delGTT
CLNSRC OMIM Allelic Variant
CLNACC RCV000043581.3,