Have questions? Visit https://www.reddit.com/r/SNPedia

rs796052484

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052484(G;T)
Make rs796052484(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28768010
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052484
ebirs796052484
HLIrs796052484
Exacrs796052484
Varsomers796052484
Maprs796052484
PheGenIrs796052484
hapmaprs796052484
1000 genomesrs796052484
hgdprs796052484
ensemblrs796052484
gopubmedrs796052484
geneviewrs796052484
scholarrs796052484
googlers796052484
pharmgkbrs796052484
gwascentralrs796052484
openSNPrs796052484
23andMers796052484
23andMe allrs796052484
SNP Nexus

SNPshotrs796052484
SNPdbers796052484
MSV3drs796052484
GWAS Ctlgrs796052484
Max Magnitude0
ClinVar
Risk rs796052484(T;T)
Alt rs796052484(T;T)
Reference rs796052484(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237216G>T
CLNSRC
CLNACC RCV000187486.1,