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rs1085307966

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome14
Position28768040
GeneFOXG1
is asnp
is mentioned by
dbSNPrs1085307966
dbSNP (old)rs1085307966
ClinGenrs1085307966
ebirs1085307966
HLIrs1085307966
Exacrs1085307966
Gnomadrs1085307966
Varsomers1085307966
Maprs1085307966
PheGenIrs1085307966
Biobankrs1085307966
1000 genomesrs1085307966
hgdprs1085307966
ensemblrs1085307966
gopubmedrs1085307966
geneviewrs1085307966
scholarrs1085307966
googlers1085307966
pharmgkbrs1085307966
gwascentralrs1085307966
openSNPrs1085307966
23andMers1085307966
23andMe allrs1085307966
SNPshotrs1085307966
SNPdbers1085307966
MSV3drs1085307966
GWAS Ctlgrs1085307966
Max Magnitude0
ClinVar
Risk rs1085307966(G;G)
Alt rs1085307966(G;G)
Reference Rs1085307966(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237246A>G
CLNSRC
CLNACC RCV000489969.1,