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rs1060501487

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1060501487(-;-)
Make rs1060501487(-;G)
ReferenceGRCh38.p7 38.3/150
Chromosome22
Position31819200
GeneDEPDC5
is asnp
is mentioned by
dbSNPrs1060501487
dbSNP (old)rs1060501487
ClinGenrs1060501487
ebirs1060501487
HLIrs1060501487
Exacrs1060501487
Gnomadrs1060501487
Varsomers1060501487
Maprs1060501487
PheGenIrs1060501487
Biobankrs1060501487
1000 genomesrs1060501487
hgdprs1060501487
ensemblrs1060501487
gopubmedrs1060501487
geneviewrs1060501487
scholarrs1060501487
googlers1060501487
pharmgkbrs1060501487
gwascentralrs1060501487
openSNPrs1060501487
23andMers1060501487
23andMe allrs1060501487
SNPshotrs1060501487
SNPdbers1060501487
MSV3drs1060501487
GWAS Ctlgrs1060501487
Max Magnitude0
ClinVar
Risk rs1060501487(-;-)
Alt rs1060501487(-;-)
Reference Rs1060501487(G;G)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene DEPDC5
CLNDBN Epilepsy, familial focal, with variable foci 1
Reversed 0
HGVS NC_000022.10:g.32215186delG
CLNSRC
CLNACC RCV000457840.1,