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

rs796052458

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052458(C;T)
Make rs796052458(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767496
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052458
ebirs796052458
HLIrs796052458
Exacrs796052458
Varsomers796052458
Maprs796052458
PheGenIrs796052458
hapmaprs796052458
1000 genomesrs796052458
hgdprs796052458
ensemblrs796052458
gopubmedrs796052458
geneviewrs796052458
scholarrs796052458
googlers796052458
pharmgkbrs796052458
gwascentralrs796052458
openSNPrs796052458
23andMers796052458
23andMe allrs796052458
SNP Nexus

SNPshotrs796052458
SNPdbers796052458
MSV3drs796052458
GWAS Ctlgrs796052458
Max Magnitude0
ClinVar
Risk rs796052458(T;T)
Alt rs796052458(T;T)
Reference rs796052458(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29236702C>T
CLNSRC
CLNACC RCV000187450.1,