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rs796052476

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs796052476(-;G)
Make rs796052476(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767662
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052476
ClinGenrs796052476
ebirs796052476
HLIrs796052476
Exacrs796052476
Varsomers796052476
Maprs796052476
PheGenIrs796052476
hapmaprs796052476
1000 genomesrs796052476
hgdprs796052476
ensemblrs796052476
gopubmedrs796052476
geneviewrs796052476
scholarrs796052476
googlers796052476
pharmgkbrs796052476
gwascentralrs796052476
openSNPrs796052476
23andMers796052476
23andMe allrs796052476
SNP Nexus

SNPshotrs796052476
SNPdbers796052476
MSV3drs796052476
GWAS Ctlgrs796052476
Max Magnitude0
ClinVar
Risk rs796052476(G;G)
Alt rs796052476(G;G)
Reference Rs796052476(-;-)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29236868dupG
CLNSRC
CLNACC RCV000187478.1,