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rs1064796823

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome14
Position28767998
GeneFOXG1
is asnp
is mentioned by
dbSNPrs1064796823
dbSNP (old)rs1064796823
ClinGenrs1064796823
ebirs1064796823
HLIrs1064796823
Exacrs1064796823
Gnomadrs1064796823
Varsomers1064796823
Maprs1064796823
PheGenIrs1064796823
Biobankrs1064796823
1000 genomesrs1064796823
hgdprs1064796823
ensemblrs1064796823
gopubmedrs1064796823
geneviewrs1064796823
scholarrs1064796823
googlers1064796823
pharmgkbrs1064796823
gwascentralrs1064796823
openSNPrs1064796823
23andMers1064796823
23andMe allrs1064796823
SNPshotrs1064796823
SNPdbers1064796823
MSV3drs1064796823
GWAS Ctlgrs1064796823
Max Magnitude0
ClinVar
Risk rs1064796823(G;G)
Alt rs1064796823(G;G)
Reference Rs1064796823(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237204T>G
CLNSRC
CLNACC RCV000480860.1,