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rs796052482

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs796052482(C;C)
Make rs796052482(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767952
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052482
ebirs796052482
HLIrs796052482
Exacrs796052482
Varsomers796052482
Maprs796052482
PheGenIrs796052482
hapmaprs796052482
1000 genomesrs796052482
hgdprs796052482
ensemblrs796052482
gopubmedrs796052482
geneviewrs796052482
scholarrs796052482
googlers796052482
pharmgkbrs796052482
gwascentralrs796052482
openSNPrs796052482
23andMers796052482
23andMe allrs796052482
SNP Nexus

SNPshotrs796052482
SNPdbers796052482
MSV3drs796052482
GWAS Ctlgrs796052482
Max Magnitude0
ClinVar
Risk rs796052482(C;C)
Alt rs796052482(C;C)
Reference rs796052482(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237158T>C
CLNSRC
CLNACC RCV000187484.1,