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rs199502880

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs199502880(A;G)
Make rs199502880(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome14
Position28767965
GeneFOXG1
is asnp
is mentioned by
dbSNPrs199502880
ebirs199502880
HLIrs199502880
Exacrs199502880
Varsomers199502880
Maprs199502880
PheGenIrs199502880
hapmaprs199502880
1000 genomesrs199502880
hgdprs199502880
ensemblrs199502880
gopubmedrs199502880
geneviewrs199502880
scholarrs199502880
googlers199502880
pharmgkbrs199502880
gwascentralrs199502880
openSNPrs199502880
23andMers199502880
23andMe allrs199502880
SNP Nexus

SNPshotrs199502880
SNPdbers199502880
MSV3drs199502880
GWAS Ctlgrs199502880
Max Magnitude0
ClinVar
Risk rs199502880(G;G)
Alt rs199502880(G;G)
Reference rs199502880(A;A)
Significance Pathogenic
Disease not provided
Variation info
Gene FOXG1
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.29237171T>A
CLNSRC
CLNACC RCV000187461.1,