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rs1064796087

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position166046917
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1064796087
dbSNP (old)rs1064796087
ClinGenrs1064796087
ebirs1064796087
HLIrs1064796087
Exacrs1064796087
Gnomadrs1064796087
Varsomers1064796087
Maprs1064796087
PheGenIrs1064796087
Biobankrs1064796087
1000 genomesrs1064796087
hgdprs1064796087
ensemblrs1064796087
gopubmedrs1064796087
geneviewrs1064796087
scholarrs1064796087
googlers1064796087
pharmgkbrs1064796087
gwascentralrs1064796087
openSNPrs1064796087
23andMers1064796087
23andMe allrs1064796087
SNPshotrs1064796087
SNPdbers1064796087
MSV3drs1064796087
GWAS Ctlgrs1064796087
Max Magnitude0
ClinVar
Risk rs1064796087(-;-)
Alt rs1064796087(-;-)
Reference Rs1064796087(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166903427delG
CLNSRC
CLNACC RCV000486955.1,