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rs1064794727

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome12
Position51807092
GeneSCN8A
is asnp
is mentioned by
dbSNPrs1064794727
dbSNP (old)rs1064794727
ClinGenrs1064794727
ebirs1064794727
HLIrs1064794727
Exacrs1064794727
Gnomadrs1064794727
Varsomers1064794727
Maprs1064794727
PheGenIrs1064794727
Biobankrs1064794727
1000 genomesrs1064794727
hgdprs1064794727
ensemblrs1064794727
gopubmedrs1064794727
geneviewrs1064794727
scholarrs1064794727
googlers1064794727
pharmgkbrs1064794727
gwascentralrs1064794727
openSNPrs1064794727
23andMers1064794727
23andMe allrs1064794727
SNPshotrs1064794727
SNPdbers1064794727
MSV3drs1064794727
GWAS Ctlgrs1064794727
Max Magnitude0
ClinVar
Risk rs1064794727(C;C)
Alt rs1064794727(C;C)
Reference Rs1064794727(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN8A
CLNDBN not provided
Reversed 0
HGVS NC_000012.11:g.52200876T>C
CLNSRC
CLNACC RCV000481897.1,