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rs796052464

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052464(C;G)
Make rs796052464(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767930
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052464
ebirs796052464
HLIrs796052464
Exacrs796052464
Varsomers796052464
Maprs796052464
PheGenIrs796052464
hapmaprs796052464
1000 genomesrs796052464
hgdprs796052464
ensemblrs796052464
gopubmedrs796052464
geneviewrs796052464
scholarrs796052464
googlers796052464
pharmgkbrs796052464
gwascentralrs796052464
openSNPrs796052464
23andMers796052464
23andMe allrs796052464
SNP Nexus

SNPshotrs796052464
SNPdbers796052464
MSV3drs796052464
GWAS Ctlgrs796052464
Max Magnitude0
ClinVar
Risk rs796052464(G;G)
Alt rs796052464(G;G)
Reference rs796052464(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237136C>G
CLNSRC
CLNACC RCV000187458.1,