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rs796052467

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052467(C;T)
Make rs796052467(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767980
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052467
ebirs796052467
HLIrs796052467
Exacrs796052467
Varsomers796052467
Maprs796052467
PheGenIrs796052467
hapmaprs796052467
1000 genomesrs796052467
hgdprs796052467
ensemblrs796052467
gopubmedrs796052467
geneviewrs796052467
scholarrs796052467
googlers796052467
pharmgkbrs796052467
gwascentralrs796052467
openSNPrs796052467
23andMers796052467
23andMe allrs796052467
SNP Nexus

SNPshotrs796052467
SNPdbers796052467
MSV3drs796052467
GWAS Ctlgrs796052467
Max Magnitude0
ClinVar
Risk rs796052467(T;T)
Alt rs796052467(T;T)
Reference rs796052467(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237186C>T
CLNSRC
CLNACC RCV000187463.1,