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rs796052462

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052462(A;A)
Make rs796052462(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767840
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052462
ebirs796052462
HLIrs796052462
Exacrs796052462
Varsomers796052462
Maprs796052462
PheGenIrs796052462
hapmaprs796052462
1000 genomesrs796052462
hgdprs796052462
ensemblrs796052462
gopubmedrs796052462
geneviewrs796052462
scholarrs796052462
googlers796052462
pharmgkbrs796052462
gwascentralrs796052462
openSNPrs796052462
23andMers796052462
23andMe allrs796052462
SNP Nexus

SNPshotrs796052462
SNPdbers796052462
MSV3drs796052462
GWAS Ctlgrs796052462
Max Magnitude0
ClinVar
Risk rs796052462(A;A)
Alt rs796052462(A;A)
Reference rs796052462(C;C)
Significance Pathogenic
Disease not specified Inborn genetic diseases
Variation info
Gene FOXG1
CLNDBN not specified Inborn genetic diseases
Reversed 0
HGVS NC_000014.8:g.29237046C>A
CLNSRC
CLNACC RCV000187456.1, RCV000190704.1,