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rs541024038

From SNPedia

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Geno Mag Summary
(C;C) 0 common in clinvar
Make rs541024038(C;T)
Make rs541024038(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position31843106
GeneDEPDC5
is asnp
is mentioned by
dbSNPrs541024038
ebirs541024038
HLIrs541024038
Exacrs541024038
Varsomers541024038
Maprs541024038
PheGenIrs541024038
hapmaprs541024038
1000 genomesrs541024038
hgdprs541024038
ensemblrs541024038
gopubmedrs541024038
geneviewrs541024038
scholarrs541024038
googlers541024038
pharmgkbrs541024038
gwascentralrs541024038
openSNPrs541024038
23andMers541024038
23andMe allrs541024038
SNP Nexus

SNPshotrs541024038
SNPdbers541024038
MSV3drs541024038
GWAS Ctlgrs541024038
Max Magnitude0
ClinVar
Risk rs541024038(G,T;G,T)
Alt rs541024038(G,T;G,T)
Reference rs541024038(C;C)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene DEPDC5
CLNDBN Epilepsy, familial focal, with variable foci
Reversed 0
HGVS NC_000022.10:g.32239092C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000157606.3,