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rs866242631

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs866242631(C;T)
Make rs866242631(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome9
Position135768847
GeneKCNT1
is asnp
is mentioned by
dbSNPrs866242631
dbSNP (classic)rs866242631
ClinGenrs866242631
ebirs866242631
HLIrs866242631
Exacrs866242631
Gnomadrs866242631
Varsomers866242631
LitVarrs866242631
Maprs866242631
PheGenIrs866242631
Biobankrs866242631
1000 genomesrs866242631
hgdprs866242631
ensemblrs866242631
geneviewrs866242631
scholarrs866242631
googlers866242631
pharmgkbrs866242631
gwascentralrs866242631
openSNPrs866242631
23andMers866242631
SNPshotrs866242631
SNPdbers866242631
MSV3drs866242631
GWAS Ctlgrs866242631
Max Magnitude0
ClinVar
Risk rs866242631(A;A) rs866242631(T;T)
Alt rs866242631(A;A) rs866242631(T;T)
Reference Rs866242631(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene KCNT1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.138660693C>A; NC_000009.11:g.138660693C>T
CLNSRC
CLNACC RCV000371693.1, RCV000255800.1,