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rs1064796964

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(TAAG;TAAG) 0 common in clinvar
Chromosome2
Position166009765
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1064796964
dbSNP (old)rs1064796964
ClinGenrs1064796964
ebirs1064796964
HLIrs1064796964
Exacrs1064796964
Gnomadrs1064796964
Varsomers1064796964
Maprs1064796964
PheGenIrs1064796964
Biobankrs1064796964
1000 genomesrs1064796964
hgdprs1064796964
ensemblrs1064796964
gopubmedrs1064796964
geneviewrs1064796964
scholarrs1064796964
googlers1064796964
pharmgkbrs1064796964
gwascentralrs1064796964
openSNPrs1064796964
23andMers1064796964
23andMe allrs1064796964
SNPshotrs1064796964
SNPdbers1064796964
MSV3drs1064796964
GWAS Ctlgrs1064796964
Max Magnitude0
ClinVar
Risk rs1064796964(-;-)
Alt rs1064796964(-;-)
Reference Rs1064796964(TAAG;TAAG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166866275_166866278delCTTA
CLNSRC
CLNACC RCV000480815.1,