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rs1057518066

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518066(C;T)
Make rs1057518066(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position135765732
GeneKCNT1
is asnp
is mentioned by
dbSNPrs1057518066
dbSNP (old)rs1057518066
ClinGenrs1057518066
ebirs1057518066
HLIrs1057518066
Exacrs1057518066
Gnomadrs1057518066
Varsomers1057518066
Maprs1057518066
PheGenIrs1057518066
Biobankrs1057518066
1000 genomesrs1057518066
hgdprs1057518066
ensemblrs1057518066
gopubmedrs1057518066
geneviewrs1057518066
scholarrs1057518066
googlers1057518066
pharmgkbrs1057518066
gwascentralrs1057518066
openSNPrs1057518066
23andMers1057518066
23andMe allrs1057518066
SNPshotrs1057518066
SNPdbers1057518066
MSV3drs1057518066
GWAS Ctlgrs1057518066
Max Magnitude0
ClinVar
Risk rs1057518066(T;T)
Alt rs1057518066(T;T)
Reference Rs1057518066(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNT1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.138657578C>T
CLNSRC
CLNACC RCV000413029.1,