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rs397515405

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs397515405(C;T)
Make rs397515405(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position135779411
GeneKCNT1
is asnp
is mentioned by
dbSNPrs397515405
ebirs397515405
HLIrs397515405
Exacrs397515405
Varsomers397515405
Maprs397515405
PheGenIrs397515405
hapmaprs397515405
1000 genomesrs397515405
hgdprs397515405
ensemblrs397515405
gopubmedrs397515405
geneviewrs397515405
scholarrs397515405
googlers397515405
pharmgkbrs397515405
gwascentralrs397515405
openSNPrs397515405
23andMers397515405
23andMe allrs397515405
SNP Nexus

SNPshotrs397515405
SNPdbers397515405
MSV3drs397515405
GWAS Ctlgrs397515405
Max Magnitude0
ClinVar
Risk rs397515405(T;T)
Alt rs397515405(T;T)
Reference rs397515405(C;C)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene KCNT1
CLNDBN Epilepsy, nocturnal frontal lobe, 5
Reversed 0
HGVS NC_000009.11:g.138671257C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000032797.2,