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rs151272083

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs151272083(A;A)
Make rs151272083(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome9
Position135778822
GeneKCNT1
is asnp
is mentioned by
dbSNPrs151272083
ebirs151272083
HLIrs151272083
Exacrs151272083
Varsomers151272083
Maprs151272083
PheGenIrs151272083
hapmaprs151272083
1000 genomesrs151272083
hgdprs151272083
ensemblrs151272083
gopubmedrs151272083
geneviewrs151272083
scholarrs151272083
googlers151272083
pharmgkbrs151272083
gwascentralrs151272083
openSNPrs151272083
23andMers151272083
23andMe allrs151272083
SNP Nexus

SNPshotrs151272083
SNPdbers151272083
MSV3drs151272083
GWAS Ctlgrs151272083
Max Magnitude0
ClinVar
Risk rs151272083(A;A)
Alt rs151272083(A;A)
Reference rs151272083(G;G)
Significance Probable-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.138670668G>A
CLNSRC
CLNACC RCV000209930.1, RCV000230529.1,