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rs1057517859

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057517859(G;T)
Make rs1057517859(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position28767790
GeneFOXG1
is asnp
is mentioned by
dbSNPrs1057517859
dbSNP (old)rs1057517859
ClinGenrs1057517859
ebirs1057517859
HLIrs1057517859
Exacrs1057517859
Gnomadrs1057517859
Varsomers1057517859
Maprs1057517859
PheGenIrs1057517859
Biobankrs1057517859
1000 genomesrs1057517859
hgdprs1057517859
ensemblrs1057517859
gopubmedrs1057517859
geneviewrs1057517859
scholarrs1057517859
googlers1057517859
pharmgkbrs1057517859
gwascentralrs1057517859
openSNPrs1057517859
23andMers1057517859
23andMe allrs1057517859
SNPshotrs1057517859
SNPdbers1057517859
MSV3drs1057517859
GWAS Ctlgrs1057517859
Max Magnitude0
ClinVar
Risk rs1057517859(T;T)
Alt rs1057517859(T;T)
Reference Rs1057517859(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29236996G>T
CLNSRC
CLNACC RCV000413843.1,