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rs397515402

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515402(A;A)
Make rs397515402(A;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position135765706
GeneKCNT1
is asnp
is mentioned by
dbSNPrs397515402
ebirs397515402
HLIrs397515402
Exacrs397515402
Varsomers397515402
Maprs397515402
PheGenIrs397515402
hapmaprs397515402
1000 genomesrs397515402
hgdprs397515402
ensemblrs397515402
gopubmedrs397515402
geneviewrs397515402
scholarrs397515402
googlers397515402
pharmgkbrs397515402
gwascentralrs397515402
openSNPrs397515402
23andMers397515402
23andMe allrs397515402
SNP Nexus

SNPshotrs397515402
SNPdbers397515402
MSV3drs397515402
GWAS Ctlgrs397515402
Max Magnitude0
ClinVar
Risk rs397515402(A;A)
Alt rs397515402(A;A)
Reference rs397515402(G;G)
Significance Pathogenic
Disease Early infantile epileptic encephalopathy 14 Epilepsy
Variation info
Gene KCNT1
CLNDBN Early infantile epileptic encephalopathy 14 Epilepsy, nocturnal frontal lobe, 5
Reversed 0
HGVS NC_000009.11:g.138657552G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000032793.3, RCV000117358.1,