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rs796052468

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052468(A;A)
Make rs796052468(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767987
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052468
ebirs796052468
HLIrs796052468
Exacrs796052468
Varsomers796052468
Maprs796052468
PheGenIrs796052468
hapmaprs796052468
1000 genomesrs796052468
hgdprs796052468
ensemblrs796052468
gopubmedrs796052468
geneviewrs796052468
scholarrs796052468
googlers796052468
pharmgkbrs796052468
gwascentralrs796052468
openSNPrs796052468
23andMers796052468
23andMe allrs796052468
SNP Nexus

SNPshotrs796052468
SNPdbers796052468
MSV3drs796052468
GWAS Ctlgrs796052468
Max Magnitude0
ClinVar
Risk rs796052468(A;A)
Alt rs796052468(A;A)
Reference rs796052468(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237193C>A
CLNSRC
CLNACC RCV000187464.2,