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rs863224020

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs863224020(A;A)
Make rs863224020(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position126277535
GeneFOXRED1
is asnp
is mentioned by
dbSNPrs863224020
ebirs863224020
HLIrs863224020
Exacrs863224020
Varsomers863224020
Maprs863224020
PheGenIrs863224020
hapmaprs863224020
1000 genomesrs863224020
hgdprs863224020
ensemblrs863224020
gopubmedrs863224020
geneviewrs863224020
scholarrs863224020
googlers863224020
pharmgkbrs863224020
gwascentralrs863224020
openSNPrs863224020
23andMers863224020
23andMe allrs863224020
SNP Nexus

SNPshotrs863224020
SNPdbers863224020
MSV3drs863224020
GWAS Ctlgrs863224020
Max Magnitude0
ClinVar
Risk rs863224020(A;A)
Alt rs863224020(A;A)
Reference rs863224020(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene FOXRED1
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.126147430G>A
CLNSRC
CLNACC RCV000198058.1,