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rs1064794913

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome2
Position166045072
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1064794913
dbSNP (old)rs1064794913
ClinGenrs1064794913
ebirs1064794913
HLIrs1064794913
Exacrs1064794913
Gnomadrs1064794913
Varsomers1064794913
Maprs1064794913
PheGenIrs1064794913
Biobankrs1064794913
1000 genomesrs1064794913
hgdprs1064794913
ensemblrs1064794913
gopubmedrs1064794913
geneviewrs1064794913
scholarrs1064794913
googlers1064794913
pharmgkbrs1064794913
gwascentralrs1064794913
openSNPrs1064794913
23andMers1064794913
23andMe allrs1064794913
SNPshotrs1064794913
SNPdbers1064794913
MSV3drs1064794913
GWAS Ctlgrs1064794913
Max Magnitude0
ClinVar
Risk rs1064794913(C;C)
Alt rs1064794913(C;C)
Reference Rs1064794913(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166901582A>G
CLNSRC
CLNACC RCV000480519.1,