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

rs397518459

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397518459(G;T)
Make rs397518459(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position100184711
GeneSPAG1
is asnp
is mentioned by
dbSNPrs397518459
ebirs397518459
HLIrs397518459
Exacrs397518459
Varsomers397518459
Maprs397518459
PheGenIrs397518459
hapmaprs397518459
1000 genomesrs397518459
hgdprs397518459
ensemblrs397518459
gopubmedrs397518459
geneviewrs397518459
scholarrs397518459
googlers397518459
pharmgkbrs397518459
gwascentralrs397518459
openSNPrs397518459
23andMers397518459
23andMe allrs397518459
SNP Nexus

SNPshotrs397518459
SNPdbers397518459
MSV3drs397518459
GWAS Ctlgrs397518459
Max Magnitude0
ClinVar
Risk rs397518459(T;T)
Alt rs397518459(T;T)
Reference rs397518459(G;G)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene SPAG1
CLNDBN Epilepsy, nocturnal frontal lobe, 5
Reversed 0
HGVS NC_000008.10:g.101196939G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000074365.4,