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rs797044545

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs797044545(A;G)
Make rs797044545(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position31838683
GeneDEPDC5
is asnp
is mentioned by
dbSNPrs797044545
ebirs797044545
HLIrs797044545
Exacrs797044545
Varsomers797044545
Maprs797044545
PheGenIrs797044545
hapmaprs797044545
1000 genomesrs797044545
hgdprs797044545
ensemblrs797044545
gopubmedrs797044545
geneviewrs797044545
scholarrs797044545
googlers797044545
pharmgkbrs797044545
gwascentralrs797044545
openSNPrs797044545
23andMers797044545
23andMe allrs797044545
SNP Nexus

SNPshotrs797044545
SNPdbers797044545
MSV3drs797044545
GWAS Ctlgrs797044545
Max Magnitude0
ClinVar
Risk rs797044545(G;G)
Alt rs797044545(G;G)
Reference rs797044545(A;A)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene DEPDC5
CLNDBN Epilepsy, familial focal, with variable foci
Reversed 0
HGVS NC_000022.10:g.32234669A>G
CLNSRC
CLNACC RCV000192061.1,