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rs1085307892

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome2
Position166051865
GeneSCN1A
is asnp
is mentioned by
dbSNPrs1085307892
dbSNP (old)rs1085307892
ClinGenrs1085307892
ebirs1085307892
HLIrs1085307892
Exacrs1085307892
Gnomadrs1085307892
Varsomers1085307892
Maprs1085307892
PheGenIrs1085307892
Biobankrs1085307892
1000 genomesrs1085307892
hgdprs1085307892
ensemblrs1085307892
gopubmedrs1085307892
geneviewrs1085307892
scholarrs1085307892
googlers1085307892
pharmgkbrs1085307892
gwascentralrs1085307892
openSNPrs1085307892
23andMers1085307892
23andMe allrs1085307892
SNPshotrs1085307892
SNPdbers1085307892
MSV3drs1085307892
GWAS Ctlgrs1085307892
Max Magnitude0
ClinVar
Risk rs1085307892(C;C)
Alt rs1085307892(C;C)
Reference Rs1085307892(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene SCN1A
CLNDBN not provided
Reversed 1
HGVS NC_000002.11:g.166908375A>G
CLNSRC
CLNACC RCV000489544.1,