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rs1569175

From SNPedia

Orientationminus
Stabilizedminus
Make rs1569175(A;A)
Make rs1569175(A;G)
Make rs1569175(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position200157231
is asnp
is mentioned by
dbSNPrs1569175
ebirs1569175
HLIrs1569175
Exacrs1569175
Varsomers1569175
Maprs1569175
PheGenIrs1569175
hapmaprs1569175
1000 genomesrs1569175
hgdprs1569175
ensemblrs1569175
gopubmedrs1569175
geneviewrs1569175
scholarrs1569175
googlers1569175
pharmgkbrs1569175
gwascentralrs1569175
openSNPrs1569175
23andMers1569175
23andMe allrs1569175
SNP Nexus

SNPshotrs1569175
SNPdbers1569175
MSV3drs1569175
GWAS Ctlgrs1569175
GMAF0.1607
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 19176441OA-icon.png]
Trait Treatment response for acute lymphoblastic leukemia
Title Genome-wide interrogation of germline genetic variation associated with treatment response in childhood acute lymphoblastic leukemia
Risk Allele T
P-val 9E-7
Odds Ratio 2.73 [1.52-4.93]




GET Evidence
rs1569175
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.742188
summary