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rs1085307942

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome2
Position165991900
GeneLOC102724058, SCN1A
is asnp
is mentioned by
dbSNPrs1085307942
dbSNP (old)rs1085307942
ClinGenrs1085307942
ebirs1085307942
HLIrs1085307942
Exacrs1085307942
Gnomadrs1085307942
Varsomers1085307942
Maprs1085307942
PheGenIrs1085307942
Biobankrs1085307942
1000 genomesrs1085307942
hgdprs1085307942
ensemblrs1085307942
gopubmedrs1085307942
geneviewrs1085307942
scholarrs1085307942
googlers1085307942
pharmgkbrs1085307942
gwascentralrs1085307942
openSNPrs1085307942
23andMers1085307942
23andMe allrs1085307942
SNPshotrs1085307942
SNPdbers1085307942
MSV3drs1085307942
GWAS Ctlgrs1085307942
Max Magnitude0
ClinVar
Risk rs1085307942(A;A)
Alt rs1085307942(A;A)
Reference Rs1085307942(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene LOC102724058 SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166848410G>T
CLNSRC
CLNACC RCV000489965.1,