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rs7128311

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs7128311(C;C)
Make rs7128311(C;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position20540973
GeneLOC645490
is asnp
is mentioned by
dbSNPrs7128311
ebirs7128311
HLIrs7128311
Exacrs7128311
Varsomers7128311
Maprs7128311
PheGenIrs7128311
hapmaprs7128311
1000 genomesrs7128311
hgdprs7128311
ensemblrs7128311
gopubmedrs7128311
geneviewrs7128311
scholarrs7128311
googlers7128311
pharmgkbrs7128311
gwascentralrs7128311
openSNPrs7128311
23andMers7128311
23andMe allrs7128311
SNP Nexus

SNPshotrs7128311
SNPdbers7128311
MSV3drs7128311
GWAS Ctlgrs7128311
GMAF0.1345
Max Magnitude0
? (C;C) (C;T) (T;T) 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 C
P-val 0.000005
Odds Ratio 13.90 [2.72-71.1]




GET Evidence
rs7128311
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.914062
summary