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rs1057521079

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057521079(A;A)
Make rs1057521079(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position165992362
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1057521079
dbSNP (old)rs1057521079
ClinGenrs1057521079
ebirs1057521079
HLIrs1057521079
Exacrs1057521079
Gnomadrs1057521079
Varsomers1057521079
LitVarrs1057521079
Maprs1057521079
PheGenIrs1057521079
Biobankrs1057521079
1000 genomesrs1057521079
hgdprs1057521079
ensemblrs1057521079
gopubmedrs1057521079
geneviewrs1057521079
scholarrs1057521079
googlers1057521079
pharmgkbrs1057521079
gwascentralrs1057521079
openSNPrs1057521079
23andMers1057521079
23andMe allrs1057521079
SNPshotrs1057521079
SNPdbers1057521079
MSV3drs1057521079
GWAS Ctlgrs1057521079
Max Magnitude0
ClinVar
Risk rs1057521079(A;A)
Alt rs1057521079(A;A)
Reference Rs1057521079(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848872A>T
CLNSRC
CLNACC RCV000417978.1,