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rs1064794752

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome9
Position135765649
GeneKCNT1
is asnp
is mentioned by
dbSNPrs1064794752
dbSNP (classic)rs1064794752
ClinGenrs1064794752
ebirs1064794752
HLIrs1064794752
Exacrs1064794752
Gnomadrs1064794752
Varsomers1064794752
LitVarrs1064794752
Maprs1064794752
PheGenIrs1064794752
Biobankrs1064794752
1000 genomesrs1064794752
hgdprs1064794752
ensemblrs1064794752
geneviewrs1064794752
scholarrs1064794752
googlers1064794752
pharmgkbrs1064794752
gwascentralrs1064794752
openSNPrs1064794752
23andMers1064794752
23andMe allrs1064794752
SNPshotrs1064794752
SNPdbers1064794752
MSV3drs1064794752
GWAS Ctlgrs1064794752
Max Magnitude0
ClinVar
Risk rs1064794752(T;T)
Alt rs1064794752(T;T)
Reference Rs1064794752(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNT1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.138657495C>T
CLNSRC
CLNACC RCV000484142.1,