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rs2089222

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs2089222(A;A)
Make rs2089222(A;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position116564853
GeneMAP1LC3B2
is asnp
is mentioned by
dbSNPrs2089222
ebirs2089222
HLIrs2089222
Exacrs2089222
Varsomers2089222
Maprs2089222
PheGenIrs2089222
hapmaprs2089222
1000 genomesrs2089222
hgdprs2089222
ensemblrs2089222
gopubmedrs2089222
geneviewrs2089222
scholarrs2089222
googlers2089222
pharmgkbrs2089222
gwascentralrs2089222
openSNPrs2089222
23andMers2089222
23andMe allrs2089222
SNP Nexus

SNPshotrs2089222
SNPdbers2089222
MSV3drs2089222
GWAS Ctlgrs2089222
GMAF0.174
Max Magnitude0
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19684603OA-icon.png]
Trait Acute lymphoblastic leukemia (childhood)
Title Germline genomic variants associated with childhood acute lymphoblastic leukemia
Risk Allele A
P-val 8E-8
Odds Ratio 2.26 [1.60-3.0]


GET Evidence
rs2089222
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.09375
summary