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rs1057523641

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057523641(C;C)
Make rs1057523641(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position135784535
GeneKCNT1, LOC107987139
is asnp
is mentioned by
dbSNPrs1057523641
dbSNP (old)rs1057523641
ClinGenrs1057523641
ebirs1057523641
HLIrs1057523641
Exacrs1057523641
Gnomadrs1057523641
Varsomers1057523641
Maprs1057523641
PheGenIrs1057523641
Biobankrs1057523641
1000 genomesrs1057523641
hgdprs1057523641
ensemblrs1057523641
gopubmedrs1057523641
geneviewrs1057523641
scholarrs1057523641
googlers1057523641
pharmgkbrs1057523641
gwascentralrs1057523641
openSNPrs1057523641
23andMers1057523641
23andMe allrs1057523641
SNPshotrs1057523641
SNPdbers1057523641
MSV3drs1057523641
GWAS Ctlgrs1057523641
Max Magnitude0
ClinVar
Risk rs1057523641(C;C)
Alt rs1057523641(C;C)
Reference Rs1057523641(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNT1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.138676381T>C
CLNSRC
CLNACC RCV000443900.1,