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rs796052469

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052469(A;A)
Make rs796052469(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28768091
GeneFOXG1
is asnp
is mentioned by
dbSNPrs796052469
ebirs796052469
HLIrs796052469
Exacrs796052469
Varsomers796052469
Maprs796052469
PheGenIrs796052469
hapmaprs796052469
1000 genomesrs796052469
hgdprs796052469
ensemblrs796052469
gopubmedrs796052469
geneviewrs796052469
scholarrs796052469
googlers796052469
pharmgkbrs796052469
gwascentralrs796052469
openSNPrs796052469
23andMers796052469
23andMe allrs796052469
SNP Nexus

SNPshotrs796052469
SNPdbers796052469
MSV3drs796052469
GWAS Ctlgrs796052469
Max Magnitude0
ClinVar
Risk rs796052469(A;A)
Alt rs796052469(A;A)
Reference rs796052469(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.29237297G>A
CLNSRC
CLNACC RCV000187466.1,