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rs796052481

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052481(A;A)
Make rs796052481(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767950
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052481
ebirs796052481
HLIrs796052481
Exacrs796052481
Varsomers796052481
Maprs796052481
PheGenIrs796052481
hapmaprs796052481
1000 genomesrs796052481
hgdprs796052481
ensemblrs796052481
gopubmedrs796052481
geneviewrs796052481
scholarrs796052481
googlers796052481
pharmgkbrs796052481
gwascentralrs796052481
openSNPrs796052481
23andMers796052481
23andMe allrs796052481
SNP Nexus

SNPshotrs796052481
SNPdbers796052481
MSV3drs796052481
GWAS Ctlgrs796052481
Max Magnitude0
ClinVar
Risk rs796052481(A;A)
Alt rs796052481(A;A)
Reference rs796052481(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237156G>A
CLNSRC
CLNACC RCV000187483.2,