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rs796052463

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052463(C;T)
Make rs796052463(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767865
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052463
ebirs796052463
HLIrs796052463
Exacrs796052463
Varsomers796052463
Maprs796052463
PheGenIrs796052463
hapmaprs796052463
1000 genomesrs796052463
hgdprs796052463
ensemblrs796052463
gopubmedrs796052463
geneviewrs796052463
scholarrs796052463
googlers796052463
pharmgkbrs796052463
gwascentralrs796052463
openSNPrs796052463
23andMers796052463
23andMe allrs796052463
SNP Nexus

SNPshotrs796052463
SNPdbers796052463
MSV3drs796052463
GWAS Ctlgrs796052463
Max Magnitude0
ClinVar
Risk rs796052463(T;T)
Alt rs796052463(T;T)
Reference rs796052463(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237071C>T
CLNSRC
CLNACC RCV000187457.1,