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

rs796052486

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CTGT;CTGT) 0 common in clinvar
Make rs796052486(-;-)
Make rs796052486(-;TCTG)
Make rs796052486(TCTG;TCTG)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28768681
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052486
dbSNP (old)rs796052486
ClinGenrs796052486
ebirs796052486
HLIrs796052486
Exacrs796052486
Gnomadrs796052486
Varsomers796052486
Maprs796052486
PheGenIrs796052486
Biobankrs796052486
1000 genomesrs796052486
hgdprs796052486
ensemblrs796052486
gopubmedrs796052486
geneviewrs796052486
scholarrs796052486
googlers796052486
pharmgkbrs796052486
gwascentralrs796052486
openSNPrs796052486
23andMers796052486
23andMe allrs796052486
SNP Nexus

SNPshotrs796052486
SNPdbers796052486
MSV3drs796052486
GWAS Ctlgrs796052486
Max Magnitude0
ClinVar
Risk rs796052486(-;-)
Alt rs796052486(-;-)
Reference Rs796052486(CTGT;CTGT)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237887_29237890delTCTG
CLNSRC
CLNACC RCV000187489.1,