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rs1057522978

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057522978(A;G)
Make rs1057522978(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome9
Position135770972
GeneKCNT1
is asnp
is mentioned by
dbSNPrs1057522978
dbSNP (classic)rs1057522978
ClinGenrs1057522978
ebirs1057522978
HLIrs1057522978
Exacrs1057522978
Gnomadrs1057522978
Varsomers1057522978
LitVarrs1057522978
Maprs1057522978
PheGenIrs1057522978
Biobankrs1057522978
1000 genomesrs1057522978
hgdprs1057522978
ensemblrs1057522978
geneviewrs1057522978
scholarrs1057522978
googlers1057522978
pharmgkbrs1057522978
gwascentralrs1057522978
openSNPrs1057522978
23andMers1057522978
23andMe allrs1057522978
SNPshotrs1057522978
SNPdbers1057522978
MSV3drs1057522978
GWAS Ctlgrs1057522978
Max Magnitude0
ClinVar
Risk rs1057522978(G;G)
Alt rs1057522978(G;G)
Reference Rs1057522978(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene KCNT1
CLNDBN not provided
Reversed 0
HGVS NC_000009.11:g.138662818A>G
CLNSRC
CLNACC RCV000425973.1,