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rs587776973

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs587776973(C;T)
Make rs587776973(T;T)
ReferenceGRCh38 38.1/142
Chromosome22
Position31815209
GeneDEPDC5
is asnp
is mentioned by
dbSNPrs587776973
ebirs587776973
HLIrs587776973
Exacrs587776973
Varsomers587776973
Maprs587776973
PheGenIrs587776973
hapmaprs587776973
1000 genomesrs587776973
hgdprs587776973
ensemblrs587776973
gopubmedrs587776973
geneviewrs587776973
scholarrs587776973
googlers587776973
pharmgkbrs587776973
gwascentralrs587776973
openSNPrs587776973
23andMers587776973
23andMe allrs587776973
SNP Nexus

SNPshotrs587776973
SNPdbers587776973
MSV3drs587776973
GWAS Ctlgrs587776973
Max Magnitude0
ClinVar
Risk rs587776973(G,T;G,T)
Alt rs587776973(G,T;G,T)
Reference rs587776973(C;C)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene DEPDC5
CLNDBN Epilepsy, familial focal, with variable foci
Reversed 0
HGVS NC_000022.10:g.32211195C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000043580.2,