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rs1064796824

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position166046784
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1064796824
dbSNP (classic)rs1064796824
ClinGenrs1064796824
ebirs1064796824
HLIrs1064796824
Exacrs1064796824
Gnomadrs1064796824
Varsomers1064796824
LitVarrs1064796824
Maprs1064796824
PheGenIrs1064796824
Biobankrs1064796824
1000 genomesrs1064796824
hgdprs1064796824
ensemblrs1064796824
geneviewrs1064796824
scholarrs1064796824
googlers1064796824
pharmgkbrs1064796824
gwascentralrs1064796824
openSNPrs1064796824
23andMers1064796824
23andMe allrs1064796824
SNPshotrs1064796824
SNPdbers1064796824
MSV3drs1064796824
GWAS Ctlgrs1064796824
Max Magnitude0
ClinVar
Risk rs1064796824(T;T)
Alt rs1064796824(T;T)
Reference Rs1064796824(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166903294G>A
CLNSRC
CLNACC RCV000485033.1,