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rs1064795579

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome2
Position165991769
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1064795579
dbSNP (old)rs1064795579
ClinGenrs1064795579
ebirs1064795579
HLIrs1064795579
Exacrs1064795579
Gnomadrs1064795579
Varsomers1064795579
Maprs1064795579
PheGenIrs1064795579
Biobankrs1064795579
1000 genomesrs1064795579
hgdprs1064795579
ensemblrs1064795579
gopubmedrs1064795579
geneviewrs1064795579
scholarrs1064795579
googlers1064795579
pharmgkbrs1064795579
gwascentralrs1064795579
openSNPrs1064795579
23andMers1064795579
23andMe allrs1064795579
SNPshotrs1064795579
SNPdbers1064795579
MSV3drs1064795579
GWAS Ctlgrs1064795579
Max Magnitude0
ClinVar
Risk rs1064795579(T;T)
Alt rs1064795579(T;T)
Reference Rs1064795579(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848279C>A
CLNSRC
CLNACC RCV000483871.1,