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rs1057520663

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057520663(G;T)
Make rs1057520663(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position28767685
GeneFOXG1
is asnp
is mentioned by
dbSNPrs1057520663
dbSNP (old)rs1057520663
ClinGenrs1057520663
ebirs1057520663
HLIrs1057520663
Exacrs1057520663
Gnomadrs1057520663
Varsomers1057520663
LitVarrs1057520663
Maprs1057520663
PheGenIrs1057520663
Biobankrs1057520663
1000 genomesrs1057520663
hgdprs1057520663
ensemblrs1057520663
gopubmedrs1057520663
geneviewrs1057520663
scholarrs1057520663
googlers1057520663
pharmgkbrs1057520663
gwascentralrs1057520663
openSNPrs1057520663
23andMers1057520663
23andMe allrs1057520663
SNPshotrs1057520663
SNPdbers1057520663
MSV3drs1057520663
GWAS Ctlgrs1057520663
Max Magnitude0
ClinVar
Risk rs1057520663(T;T)
Alt rs1057520663(T;T)
Reference Rs1057520663(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29236891G>T
CLNSRC
CLNACC RCV000425305.1,