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rs11155133

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs11155133(A;G)
Make rs11155133(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position140848688
GeneLOC102723724
is asnp
is mentioned by
dbSNPrs11155133
ebirs11155133
HLIrs11155133
Exacrs11155133
Varsomers11155133
Maprs11155133
PheGenIrs11155133
hapmaprs11155133
1000 genomesrs11155133
hgdprs11155133
ensemblrs11155133
gopubmedrs11155133
geneviewrs11155133
scholarrs11155133
googlers11155133
pharmgkbrs11155133
gwascentralrs11155133
openSNPrs11155133
23andMers11155133
23andMe allrs11155133
SNP Nexus

SNPshotrs11155133
SNPdbers11155133
MSV3drs11155133
GWAS Ctlgrs11155133
GMAF0.1116
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 G
P-val 3E-7
Odds Ratio 3.62 [2.10-6.00]


GET Evidence
rs11155133
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.164062
summary



[PMID 26177813] Replication analysis confirms the association of several variants with acute myeloid leukemia in Chinese population