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

rs1064794495

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(AGCT;AGCT) 0 common in clinvar
Chromosome2
Position166015706
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1064794495
dbSNP (old)rs1064794495
ClinGenrs1064794495
ebirs1064794495
HLIrs1064794495
Exacrs1064794495
Gnomadrs1064794495
Varsomers1064794495
Maprs1064794495
PheGenIrs1064794495
Biobankrs1064794495
1000 genomesrs1064794495
hgdprs1064794495
ensemblrs1064794495
gopubmedrs1064794495
geneviewrs1064794495
scholarrs1064794495
googlers1064794495
pharmgkbrs1064794495
gwascentralrs1064794495
openSNPrs1064794495
23andMers1064794495
23andMe allrs1064794495
SNPshotrs1064794495
SNPdbers1064794495
MSV3drs1064794495
GWAS Ctlgrs1064794495
Max Magnitude0
ClinVar
Risk rs1064794495(-;-)
Alt rs1064794495(-;-)
Reference Rs1064794495(AGCT;AGCT)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166872216_166872219delAGCT
CLNSRC
CLNACC RCV000481280.1,