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rs6971925

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs6971925(C;T)
Make rs6971925(T;T)
ReferenceGRCh38 38.1/141
Chromosome7
Position14406292
GeneDGKB
is asnp
is mentioned by
dbSNPrs6971925
ebirs6971925
HLIrs6971925
Exacrs6971925
Varsomers6971925
Maprs6971925
PheGenIrs6971925
hapmaprs6971925
1000 genomesrs6971925
hgdprs6971925
ensemblrs6971925
gopubmedrs6971925
geneviewrs6971925
scholarrs6971925
googlers6971925
pharmgkbrs6971925
gwascentralrs6971925
openSNPrs6971925
23andMers6971925
23andMe allrs6971925
SNP Nexus

SNPshotrs6971925
SNPdbers6971925
MSV3drs6971925
GWAS Ctlgrs6971925
GMAF0.04729
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 T
P-val 0.000003
Odds Ratio 13.91 [2.72-70.92]




GET Evidence
rs6971925
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.953125
summary