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rs1064794782

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome12
Position51699632
GeneSCN8A
is asnp
is mentioned by
dbSNPrs1064794782
dbSNP (old)rs1064794782
ClinGenrs1064794782
ebirs1064794782
HLIrs1064794782
Exacrs1064794782
Gnomadrs1064794782
Varsomers1064794782
Maprs1064794782
PheGenIrs1064794782
Biobankrs1064794782
1000 genomesrs1064794782
hgdprs1064794782
ensemblrs1064794782
gopubmedrs1064794782
geneviewrs1064794782
scholarrs1064794782
googlers1064794782
pharmgkbrs1064794782
gwascentralrs1064794782
openSNPrs1064794782
23andMers1064794782
23andMe allrs1064794782
SNPshotrs1064794782
SNPdbers1064794782
MSV3drs1064794782
GWAS Ctlgrs1064794782
Max Magnitude0
ClinVar
Risk rs1064794782(G;G)
Alt rs1064794782(G;G)
Reference Rs1064794782(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52093416C>G
CLNSRC
CLNACC RCV000478102.1,