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rs1057521783

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521783(C;T)
Make rs1057521783(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position28768469
GeneFOXG1
is asnp
is mentioned by
dbSNPrs1057521783
dbSNP (old)rs1057521783
ClinGenrs1057521783
ebirs1057521783
HLIrs1057521783
Exacrs1057521783
Gnomadrs1057521783
Varsomers1057521783
LitVarrs1057521783
Maprs1057521783
PheGenIrs1057521783
Biobankrs1057521783
1000 genomesrs1057521783
hgdprs1057521783
ensemblrs1057521783
gopubmedrs1057521783
geneviewrs1057521783
scholarrs1057521783
googlers1057521783
pharmgkbrs1057521783
gwascentralrs1057521783
openSNPrs1057521783
23andMers1057521783
23andMe allrs1057521783
SNPshotrs1057521783
SNPdbers1057521783
MSV3drs1057521783
GWAS Ctlgrs1057521783
Max Magnitude0
ClinVar
Risk rs1057521783(T;T)
Alt rs1057521783(T;T)
Reference Rs1057521783(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237675C>T
CLNSRC
CLNACC RCV000439955.1,