Have questions? Visit https://www.reddit.com/r/SNPedia

rs17007695

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs17007695(C;C)
Make rs17007695(C;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position141788570
is asnp
is mentioned by
dbSNPrs17007695
ebirs17007695
HLIrs17007695
Exacrs17007695
Varsomers17007695
Maprs17007695
PheGenIrs17007695
hapmaprs17007695
1000 genomesrs17007695
hgdprs17007695
ensemblrs17007695
gopubmedrs17007695
geneviewrs17007695
scholarrs17007695
googlers17007695
pharmgkbrs17007695
gwascentralrs17007695
openSNPrs17007695
23andMers17007695
23andMe allrs17007695
SNP Nexus

SNPshotrs17007695
SNPdbers17007695
MSV3drs17007695
GWAS Ctlgrs17007695
GMAF0.1809
Max Magnitude0
? (C;C) (C;T) (T;T) 28
news Leukemia
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 9E-7
Odds Ratio 2.67 [1.53-4.68]




GET Evidence
rs17007695
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.106557
summary