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rs35229355

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs35229355(C;T)
Make rs35229355(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position155608667
is asnp
is mentioned by
dbSNPrs35229355
ebirs35229355
HLIrs35229355
Exacrs35229355
Varsomers35229355
Maprs35229355
PheGenIrs35229355
hapmaprs35229355
1000 genomesrs35229355
hgdprs35229355
ensemblrs35229355
gopubmedrs35229355
geneviewrs35229355
scholarrs35229355
googlers35229355
pharmgkbrs35229355
gwascentralrs35229355
openSNPrs35229355
23andMers35229355
23andMe allrs35229355
SNP Nexus

SNPshotrs35229355
SNPdbers35229355
MSV3drs35229355
GWAS Ctlgrs35229355
GMAF0.1396
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 0.000005
Odds Ratio 7.24 [2.46-21.30]




GET Evidence
rs35229355
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.0625
summary