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rs17079534

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 2.5 Increased odds of relapse in treated childhood ALL patients
(A;G) 2 Increased odds of relapse in treated childhood ALL patients
(G;G) 0 common/normal
ReferenceGRCh38 38.1/141
Chromosome3
Position39805581
is asnp
is mentioned by
dbSNPrs17079534
ebirs17079534
HLIrs17079534
Exacrs17079534
Varsomers17079534
Maprs17079534
PheGenIrs17079534
hapmaprs17079534
1000 genomesrs17079534
hgdprs17079534
ensemblrs17079534
gopubmedrs17079534
geneviewrs17079534
scholarrs17079534
googlers17079534
pharmgkbrs17079534
gwascentralrs17079534
openSNPrs17079534
23andMers17079534
23andMe allrs17079534
SNP Nexus

SNPshotrs17079534
SNPdbers17079534
MSV3drs17079534
GWAS Ctlgrs17079534
GMAF0.0202
Max Magnitude2.5

[PMID 23007406OA-icon.png] Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia. Each rs17079534(A) allele increases odds of relapse by 4.07 (CI:2.4-6.87, adjusted p=2 × 10e−4) based on a study of 2,500 childhood acute lymphoblastic leukemia patients.

? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23007406OA-icon.png]
Trait Acute lymphoblastic leukemia (childhood)
Title Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.
Risk Allele A
P-val 2E-7
Odds Ratio 4.07 [2.40-6.87]