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rs1064794147

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome2
Position166046800
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1064794147
dbSNP (old)rs1064794147
ClinGenrs1064794147
ebirs1064794147
HLIrs1064794147
Exacrs1064794147
Gnomadrs1064794147
Varsomers1064794147
Maprs1064794147
PheGenIrs1064794147
Biobankrs1064794147
1000 genomesrs1064794147
hgdprs1064794147
ensemblrs1064794147
gopubmedrs1064794147
geneviewrs1064794147
scholarrs1064794147
googlers1064794147
pharmgkbrs1064794147
gwascentralrs1064794147
openSNPrs1064794147
23andMers1064794147
23andMe allrs1064794147
SNPshotrs1064794147
SNPdbers1064794147
MSV3drs1064794147
GWAS Ctlgrs1064794147
Max Magnitude0
ClinVar
Risk rs1064794147(-;-)
Alt rs1064794147(-;-)
Reference Rs1064794147(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166903310delT
CLNSRC
CLNACC RCV000478204.1,