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rs1064796714

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome2
Position166002596
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1064796714
dbSNP (old)rs1064796714
ClinGenrs1064796714
ebirs1064796714
HLIrs1064796714
Exacrs1064796714
Gnomadrs1064796714
Varsomers1064796714
Maprs1064796714
PheGenIrs1064796714
Biobankrs1064796714
1000 genomesrs1064796714
hgdprs1064796714
ensemblrs1064796714
gopubmedrs1064796714
geneviewrs1064796714
scholarrs1064796714
googlers1064796714
pharmgkbrs1064796714
gwascentralrs1064796714
openSNPrs1064796714
23andMers1064796714
23andMe allrs1064796714
SNPshotrs1064796714
SNPdbers1064796714
MSV3drs1064796714
GWAS Ctlgrs1064796714
Max Magnitude0
ClinVar
Risk rs1064796714(-;-)
Alt rs1064796714(-;-)
Reference Rs1064796714(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166859106delA
CLNSRC
CLNACC RCV000481049.1,