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rs397515407

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515407(A;A)
Make rs397515407(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position135765188
GeneKCNT1
is asnp
is mentioned by
dbSNPrs397515407
ebirs397515407
HLIrs397515407
Exacrs397515407
Varsomers397515407
Maprs397515407
PheGenIrs397515407
hapmaprs397515407
1000 genomesrs397515407
hgdprs397515407
ensemblrs397515407
gopubmedrs397515407
geneviewrs397515407
scholarrs397515407
googlers397515407
pharmgkbrs397515407
gwascentralrs397515407
openSNPrs397515407
23andMers397515407
23andMe allrs397515407
SNP Nexus

SNPshotrs397515407
SNPdbers397515407
MSV3drs397515407
GWAS Ctlgrs397515407
Max Magnitude0
ClinVar
Risk rs397515407(A;A)
Alt rs397515407(A;A)
Reference rs397515407(G;G)
Significance Pathogenic
Disease Epilepsy
Variation info
Gene KCNT1
CLNDBN Epilepsy, nocturnal frontal lobe, 5
Reversed 0
HGVS NC_000009.11:g.138657034G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000032799.2,