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rs1064794715

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome12
Position51688792
GeneSCN8A
is asnp
is mentioned by
dbSNPrs1064794715
dbSNP (old)rs1064794715
ClinGenrs1064794715
ebirs1064794715
HLIrs1064794715
Exacrs1064794715
Gnomadrs1064794715
Varsomers1064794715
Maprs1064794715
PheGenIrs1064794715
Biobankrs1064794715
1000 genomesrs1064794715
hgdprs1064794715
ensemblrs1064794715
gopubmedrs1064794715
geneviewrs1064794715
scholarrs1064794715
googlers1064794715
pharmgkbrs1064794715
gwascentralrs1064794715
openSNPrs1064794715
23andMers1064794715
23andMe allrs1064794715
SNPshotrs1064794715
SNPdbers1064794715
MSV3drs1064794715
GWAS Ctlgrs1064794715
Max Magnitude0
ClinVar
Risk rs1064794715(C;C)
Alt rs1064794715(C;C)
Reference Rs1064794715(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52082576T>C
CLNSRC
CLNACC RCV000484434.1,