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rs1057523858

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057523858(A;A)
Make rs1057523858(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position166047647
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1057523858
dbSNP (old)rs1057523858
ClinGenrs1057523858
ebirs1057523858
HLIrs1057523858
Exacrs1057523858
Gnomadrs1057523858
Varsomers1057523858
Maprs1057523858
PheGenIrs1057523858
Biobankrs1057523858
1000 genomesrs1057523858
hgdprs1057523858
ensemblrs1057523858
gopubmedrs1057523858
geneviewrs1057523858
scholarrs1057523858
googlers1057523858
pharmgkbrs1057523858
gwascentralrs1057523858
openSNPrs1057523858
23andMers1057523858
23andMe allrs1057523858
SNPshotrs1057523858
SNPdbers1057523858
MSV3drs1057523858
GWAS Ctlgrs1057523858
Max Magnitude0
ClinVar
Risk rs1057523858(A;A)
Alt rs1057523858(A;A)
Reference Rs1057523858(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166904157A>T
CLNSRC
CLNACC RCV000420406.1,