Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057518165

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057518165(C;G)
Make rs1057518165(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position28767924
GeneFOXG1
is asnp
is mentioned by
dbSNPrs1057518165
dbSNP (old)rs1057518165
ClinGenrs1057518165
ebirs1057518165
HLIrs1057518165
Exacrs1057518165
Gnomadrs1057518165
Varsomers1057518165
Maprs1057518165
PheGenIrs1057518165
Biobankrs1057518165
1000 genomesrs1057518165
hgdprs1057518165
ensemblrs1057518165
gopubmedrs1057518165
geneviewrs1057518165
scholarrs1057518165
googlers1057518165
pharmgkbrs1057518165
gwascentralrs1057518165
openSNPrs1057518165
23andMers1057518165
23andMe allrs1057518165
SNPshotrs1057518165
SNPdbers1057518165
MSV3drs1057518165
GWAS Ctlgrs1057518165
Max Magnitude0
ClinVar
Risk rs1057518165(G;G)
Alt rs1057518165(G;G)
Reference Rs1057518165(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237130C>G
CLNSRC
CLNACC RCV000414314.1,