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

rs797044546

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs797044546(C;T)
Make rs797044546(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome22
Position31906252
GeneDEPDC5
is asnp
is mentioned by
dbSNPrs797044546
ebirs797044546
HLIrs797044546
Exacrs797044546
Varsomers797044546
Maprs797044546
PheGenIrs797044546
hapmaprs797044546
1000 genomesrs797044546
hgdprs797044546
ensemblrs797044546
gopubmedrs797044546
geneviewrs797044546
scholarrs797044546
googlers797044546
pharmgkbrs797044546
gwascentralrs797044546
openSNPrs797044546
23andMers797044546
23andMe allrs797044546
SNP Nexus

SNPshotrs797044546
SNPdbers797044546
MSV3drs797044546
GWAS Ctlgrs797044546
Max Magnitude0
ClinVar
Risk rs797044546(T;T)
Alt rs797044546(T;T)
Reference rs797044546(C;C)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene DEPDC5
CLNDBN Epilepsy, familial focal, with variable foci
Reversed 0
HGVS NC_000022.10:g.32302238C>T
CLNSRC
CLNACC RCV000192062.1,