Have questions? Visit https://www.reddit.com/r/SNPedia

rs863224019

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs863224019(A;G)
Make rs863224019(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position126271590
GeneFOXRED1
is asnp
is mentioned by
dbSNPrs863224019
ebirs863224019
HLIrs863224019
Exacrs863224019
Varsomers863224019
Maprs863224019
PheGenIrs863224019
hapmaprs863224019
1000 genomesrs863224019
hgdprs863224019
ensemblrs863224019
gopubmedrs863224019
geneviewrs863224019
scholarrs863224019
googlers863224019
pharmgkbrs863224019
gwascentralrs863224019
openSNPrs863224019
23andMers863224019
23andMe allrs863224019
SNP Nexus

SNPshotrs863224019
SNPdbers863224019
MSV3drs863224019
GWAS Ctlgrs863224019
Max Magnitude0
ClinVar
Risk rs863224019(G;G)
Alt rs863224019(G;G)
Reference rs863224019(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXRED1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.126141485A>G
CLNSRC
CLNACC RCV000200660.1,