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rs1057522923

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057522923(G;G)
Make rs1057522923(G;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position135765056
GeneKCNT1
is asnp
is mentioned by
dbSNPrs1057522923
dbSNP (old)rs1057522923
ClinGenrs1057522923
ebirs1057522923
HLIrs1057522923
Exacrs1057522923
Gnomadrs1057522923
Varsomers1057522923
Maprs1057522923
PheGenIrs1057522923
Biobankrs1057522923
1000 genomesrs1057522923
hgdprs1057522923
ensemblrs1057522923
gopubmedrs1057522923
geneviewrs1057522923
scholarrs1057522923
googlers1057522923
pharmgkbrs1057522923
gwascentralrs1057522923
openSNPrs1057522923
23andMers1057522923
23andMe allrs1057522923
SNPshotrs1057522923
SNPdbers1057522923
MSV3drs1057522923
GWAS Ctlgrs1057522923
Max Magnitude0
ClinVar
Risk rs1057522923(G;G)
Alt rs1057522923(G;G)
Reference Rs1057522923(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNT1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.138656902T>G
CLNSRC
CLNACC RCV000438493.1,