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rs886041691

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome9
Position135769982
GeneKCNT1
is asnp
is mentioned by
dbSNPrs886041691
dbSNP (classic)rs886041691
ClinGenrs886041691
ebirs886041691
HLIrs886041691
Exacrs886041691
Gnomadrs886041691
Varsomers886041691
LitVarrs886041691
Maprs886041691
PheGenIrs886041691
Biobankrs886041691
1000 genomesrs886041691
hgdprs886041691
ensemblrs886041691
geneviewrs886041691
scholarrs886041691
googlers886041691
pharmgkbrs886041691
gwascentralrs886041691
openSNPrs886041691
23andMers886041691
SNPshotrs886041691
SNPdbers886041691
MSV3drs886041691
GWAS Ctlgrs886041691
Max Magnitude0
ClinVar
Risk rs886041691(G;G)
Alt rs886041691(G;G)
Reference Rs886041691(A;A)
Significance Pathogenic
Disease not provided Malignant migrating partial seizures of infancy
Variation info
Gene KCNT1
CLNDBN not provided Malignant migrating partial seizures of infancy
Reversed 0
HGVS NC_000009.11:g.138661828A>G
CLNSRC
CLNACC RCV000289855.1, RCV000417014.1,