Have data from 23andMe or Ancestry? Make a report automatically with Promethease !

rs1064794766

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome2
Position165992303
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1064794766
dbSNP (old)rs1064794766
ClinGenrs1064794766
ebirs1064794766
HLIrs1064794766
Exacrs1064794766
Gnomadrs1064794766
Varsomers1064794766
Maprs1064794766
PheGenIrs1064794766
Biobankrs1064794766
1000 genomesrs1064794766
hgdprs1064794766
ensemblrs1064794766
gopubmedrs1064794766
geneviewrs1064794766
scholarrs1064794766
googlers1064794766
pharmgkbrs1064794766
gwascentralrs1064794766
openSNPrs1064794766
23andMers1064794766
23andMe allrs1064794766
SNPshotrs1064794766
SNPdbers1064794766
MSV3drs1064794766
GWAS Ctlgrs1064794766
Max Magnitude0
ClinVar
Risk rs1064794766(C;C)
Alt rs1064794766(C;C)
Reference Rs1064794766(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848813T>G
CLNSRC
CLNACC RCV000482880.1,