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

rs1064794634

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position166056406
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1064794634
dbSNP (old)rs1064794634
ClinGenrs1064794634
ebirs1064794634
HLIrs1064794634
Exacrs1064794634
Gnomadrs1064794634
Varsomers1064794634
Maprs1064794634
PheGenIrs1064794634
Biobankrs1064794634
1000 genomesrs1064794634
hgdprs1064794634
ensemblrs1064794634
gopubmedrs1064794634
geneviewrs1064794634
scholarrs1064794634
googlers1064794634
pharmgkbrs1064794634
gwascentralrs1064794634
openSNPrs1064794634
23andMers1064794634
23andMe allrs1064794634
SNPshotrs1064794634
SNPdbers1064794634
MSV3drs1064794634
GWAS Ctlgrs1064794634
Max Magnitude0
ClinVar
Risk rs1064794634(C;C)
Alt rs1064794634(C;C)
Reference Rs1064794634(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166912916C>G
CLNSRC
CLNACC RCV000486953.1,