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rs397515406

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515406(C;C)
Make rs397515406(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position135777374
GeneKCNT1
is asnp
is mentioned by
dbSNPrs397515406
ebirs397515406
HLIrs397515406
Exacrs397515406
Varsomers397515406
Maprs397515406
PheGenIrs397515406
hapmaprs397515406
1000 genomesrs397515406
hgdprs397515406
ensemblrs397515406
gopubmedrs397515406
geneviewrs397515406
scholarrs397515406
googlers397515406
pharmgkbrs397515406
gwascentralrs397515406
openSNPrs397515406
23andMers397515406
23andMe allrs397515406
SNP Nexus

SNPshotrs397515406
SNPdbers397515406
MSV3drs397515406
GWAS Ctlgrs397515406
Max Magnitude0
ClinVar
Risk rs397515406(C;C)
Alt rs397515406(C;C)
Reference rs397515406(T;T)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene KCNT1
CLNDBN Epilepsy, nocturnal frontal lobe, 5
Reversed 0
HGVS NC_000009.11:g.138669220T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000032798.2,