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rs796052483

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs796052483(A;G)
Make rs796052483(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28768000
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052483
ebirs796052483
HLIrs796052483
Exacrs796052483
Varsomers796052483
Maprs796052483
PheGenIrs796052483
hapmaprs796052483
1000 genomesrs796052483
hgdprs796052483
ensemblrs796052483
gopubmedrs796052483
geneviewrs796052483
scholarrs796052483
googlers796052483
pharmgkbrs796052483
gwascentralrs796052483
openSNPrs796052483
23andMers796052483
23andMe allrs796052483
SNP Nexus

SNPshotrs796052483
SNPdbers796052483
MSV3drs796052483
GWAS Ctlgrs796052483
Max Magnitude0
ClinVar
Risk rs796052483(G;G)
Alt rs796052483(G;G)
Reference rs796052483(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237206A>G
CLNSRC
CLNACC RCV000187485.1,