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rs1057522914

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057522914(A;A)
Make rs1057522914(A;C)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position135758495
GeneKCNT1
is asnp
is mentioned by
dbSNPrs1057522914
dbSNP (old)rs1057522914
ClinGenrs1057522914
ebirs1057522914
HLIrs1057522914
Exacrs1057522914
Gnomadrs1057522914
Varsomers1057522914
LitVarrs1057522914
Maprs1057522914
PheGenIrs1057522914
Biobankrs1057522914
1000 genomesrs1057522914
hgdprs1057522914
ensemblrs1057522914
gopubmedrs1057522914
geneviewrs1057522914
scholarrs1057522914
googlers1057522914
pharmgkbrs1057522914
gwascentralrs1057522914
openSNPrs1057522914
23andMers1057522914
23andMe allrs1057522914
SNPshotrs1057522914
SNPdbers1057522914
MSV3drs1057522914
GWAS Ctlgrs1057522914
Max Magnitude0
ClinVar
Risk rs1057522914(A;A)
Alt rs1057522914(A;A)
Reference Rs1057522914(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNT1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.138650341C>A
CLNSRC
CLNACC RCV000418409.1,