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rs796052466

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052466(A;A)
Make rs796052466(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767954
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052466
ebirs796052466
HLIrs796052466
Exacrs796052466
Varsomers796052466
Maprs796052466
PheGenIrs796052466
hapmaprs796052466
1000 genomesrs796052466
hgdprs796052466
ensemblrs796052466
gopubmedrs796052466
geneviewrs796052466
scholarrs796052466
googlers796052466
pharmgkbrs796052466
gwascentralrs796052466
openSNPrs796052466
23andMers796052466
23andMe allrs796052466
SNP Nexus

SNPshotrs796052466
SNPdbers796052466
MSV3drs796052466
GWAS Ctlgrs796052466
Max Magnitude0
ClinVar
Risk rs796052466(A;A)
Alt rs796052466(A;A)
Reference rs796052466(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237160G>A
CLNSRC
CLNACC RCV000187460.1,