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rs1064794252

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(TG;TG) 0 common in clinvar
Chromosome2
Position166051789
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1064794252
dbSNP (old)rs1064794252
ClinGenrs1064794252
ebirs1064794252
HLIrs1064794252
Exacrs1064794252
Gnomadrs1064794252
Varsomers1064794252
LitVarrs1064794252
Maprs1064794252
PheGenIrs1064794252
Biobankrs1064794252
1000 genomesrs1064794252
hgdprs1064794252
ensemblrs1064794252
gopubmedrs1064794252
geneviewrs1064794252
scholarrs1064794252
googlers1064794252
pharmgkbrs1064794252
gwascentralrs1064794252
openSNPrs1064794252
23andMers1064794252
23andMe allrs1064794252
SNPshotrs1064794252
SNPdbers1064794252
MSV3drs1064794252
GWAS Ctlgrs1064794252
Max Magnitude0
ClinVar
Risk rs1064794252(-;-)
Alt rs1064794252(-;-)
Reference Rs1064794252(TG;TG)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166908299_166908300delCA
CLNSRC
CLNACC RCV000486831.1,