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rs796052474

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796052474(-;C)
Make rs796052474(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767518
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052474
dbSNP (old)rs796052474
ClinGenrs796052474
ebirs796052474
HLIrs796052474
Exacrs796052474
Gnomadrs796052474
Varsomers796052474
Maprs796052474
PheGenIrs796052474
Biobankrs796052474
1000 genomesrs796052474
hgdprs796052474
ensemblrs796052474
gopubmedrs796052474
geneviewrs796052474
scholarrs796052474
googlers796052474
pharmgkbrs796052474
gwascentralrs796052474
openSNPrs796052474
23andMers796052474
23andMe allrs796052474
SNP Nexus

SNPshotrs796052474
SNPdbers796052474
MSV3drs796052474
GWAS Ctlgrs796052474
Max Magnitude0
ClinVar
Risk rs796052474(C;C)
Alt rs796052474(C;C)
Reference Rs796052474(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29236724dupC
CLNSRC
CLNACC RCV000187474.1,