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rs796052465

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052465(C;T)
Make rs796052465(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767946
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052465
ebirs796052465
HLIrs796052465
Exacrs796052465
Varsomers796052465
Maprs796052465
PheGenIrs796052465
hapmaprs796052465
1000 genomesrs796052465
hgdprs796052465
ensemblrs796052465
gopubmedrs796052465
geneviewrs796052465
scholarrs796052465
googlers796052465
pharmgkbrs796052465
gwascentralrs796052465
openSNPrs796052465
23andMers796052465
23andMe allrs796052465
SNP Nexus

SNPshotrs796052465
SNPdbers796052465
MSV3drs796052465
GWAS Ctlgrs796052465
Max Magnitude0
ClinVar
Risk rs796052465(T;T)
Alt rs796052465(T;T)
Reference rs796052465(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237152C>T
CLNSRC
CLNACC RCV000187459.2,