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rs1064797030

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Chromosome14
Position28767864
GeneFOXG1
is asnp
is mentioned by
dbSNPrs1064797030
dbSNP (old)rs1064797030
ClinGenrs1064797030
ebirs1064797030
HLIrs1064797030
Exacrs1064797030
Gnomadrs1064797030
Varsomers1064797030
Maprs1064797030
PheGenIrs1064797030
Biobankrs1064797030
1000 genomesrs1064797030
hgdprs1064797030
ensemblrs1064797030
gopubmedrs1064797030
geneviewrs1064797030
scholarrs1064797030
googlers1064797030
pharmgkbrs1064797030
gwascentralrs1064797030
openSNPrs1064797030
23andMers1064797030
23andMe allrs1064797030
SNPshotrs1064797030
SNPdbers1064797030
MSV3drs1064797030
GWAS Ctlgrs1064797030
Max Magnitude0
ClinVar
Risk rs1064797030(TT;TT)
Alt rs1064797030(TT;TT)
Reference Rs1064797030(GC;GC)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237070_29237071delGCinsTT
CLNSRC
CLNACC RCV000480058.1,