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rs1064796384

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome2
Position166058603
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1064796384
dbSNP (old)rs1064796384
ClinGenrs1064796384
ebirs1064796384
HLIrs1064796384
Exacrs1064796384
Gnomadrs1064796384
Varsomers1064796384
Maprs1064796384
PheGenIrs1064796384
Biobankrs1064796384
1000 genomesrs1064796384
hgdprs1064796384
ensemblrs1064796384
gopubmedrs1064796384
geneviewrs1064796384
scholarrs1064796384
googlers1064796384
pharmgkbrs1064796384
gwascentralrs1064796384
openSNPrs1064796384
23andMers1064796384
23andMe allrs1064796384
SNPshotrs1064796384
SNPdbers1064796384
MSV3drs1064796384
GWAS Ctlgrs1064796384
Max Magnitude0
ClinVar
Risk rs1064796384(C;C)
Alt rs1064796384(C;C)
Reference Rs1064796384(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166915113A>G
CLNSRC
CLNACC RCV000481610.1,