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rs1057520780

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520780(G;T)
Make rs1057520780(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position28767739
GeneFOXG1
is asnp
is mentioned by
dbSNPrs1057520780
dbSNP (old)rs1057520780
ClinGenrs1057520780
ebirs1057520780
HLIrs1057520780
Exacrs1057520780
Gnomadrs1057520780
Varsomers1057520780
LitVarrs1057520780
Maprs1057520780
PheGenIrs1057520780
Biobankrs1057520780
1000 genomesrs1057520780
hgdprs1057520780
ensemblrs1057520780
gopubmedrs1057520780
geneviewrs1057520780
scholarrs1057520780
googlers1057520780
pharmgkbrs1057520780
gwascentralrs1057520780
openSNPrs1057520780
23andMers1057520780
23andMe allrs1057520780
SNPshotrs1057520780
SNPdbers1057520780
MSV3drs1057520780
GWAS Ctlgrs1057520780
Max Magnitude0
ClinVar
Risk rs1057520780(T;T)
Alt rs1057520780(T;T)
Reference Rs1057520780(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29236945G>T
CLNSRC
CLNACC RCV000429306.1,