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rs796052485

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GC;GC) 0 common in clinvar
Make rs796052485(ACCG;ACCG)
Make rs796052485(ACCG;GC)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767504
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052485
ClinGenrs796052485
ebirs796052485
HLIrs796052485
Exacrs796052485
Varsomers796052485
Maprs796052485
PheGenIrs796052485
hapmaprs796052485
1000 genomesrs796052485
hgdprs796052485
ensemblrs796052485
gopubmedrs796052485
geneviewrs796052485
scholarrs796052485
googlers796052485
pharmgkbrs796052485
gwascentralrs796052485
openSNPrs796052485
23andMers796052485
23andMe allrs796052485
SNP Nexus

SNPshotrs796052485
SNPdbers796052485
MSV3drs796052485
GWAS Ctlgrs796052485
Max Magnitude0
ClinVar
Risk rs796052485(ACCG;ACCG)
Alt rs796052485(ACCG;ACCG)
Reference Rs796052485(GC;GC)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29236710_29236711delGCinsACCG
CLNSRC
CLNACC RCV000187487.1,