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rs1064794508

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position166041332
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1064794508
dbSNP (old)rs1064794508
ClinGenrs1064794508
ebirs1064794508
HLIrs1064794508
Exacrs1064794508
Gnomadrs1064794508
Varsomers1064794508
Maprs1064794508
PheGenIrs1064794508
Biobankrs1064794508
1000 genomesrs1064794508
hgdprs1064794508
ensemblrs1064794508
gopubmedrs1064794508
geneviewrs1064794508
scholarrs1064794508
googlers1064794508
pharmgkbrs1064794508
gwascentralrs1064794508
openSNPrs1064794508
23andMers1064794508
23andMe allrs1064794508
SNPshotrs1064794508
SNPdbers1064794508
MSV3drs1064794508
GWAS Ctlgrs1064794508
Max Magnitude0
ClinVar
Risk rs1064794508(-;-)
Alt rs1064794508(-;-)
Reference Rs1064794508(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166897842delG
CLNSRC
CLNACC RCV000479576.1,