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rs1064795355

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome2
Position166012188
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1064795355
dbSNP (old)rs1064795355
ClinGenrs1064795355
ebirs1064795355
HLIrs1064795355
Exacrs1064795355
Gnomadrs1064795355
Varsomers1064795355
LitVarrs1064795355
Maprs1064795355
PheGenIrs1064795355
Biobankrs1064795355
1000 genomesrs1064795355
hgdprs1064795355
ensemblrs1064795355
gopubmedrs1064795355
geneviewrs1064795355
scholarrs1064795355
googlers1064795355
pharmgkbrs1064795355
gwascentralrs1064795355
openSNPrs1064795355
23andMers1064795355
23andMe allrs1064795355
SNPshotrs1064795355
SNPdbers1064795355
MSV3drs1064795355
GWAS Ctlgrs1064795355
Max Magnitude0
ClinVar
Risk rs1064795355(C;C)
Alt rs1064795355(C;C)
Reference Rs1064795355(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166868698A>G
CLNSRC
CLNACC RCV000478580.1,