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rs7115578

From SNPedia

Orientationplus
Stabilizedplus
Make rs7115578(A;A)
Make rs7115578(A;G)
Make rs7115578(G;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position96266936
GeneMAML2
is asnp
is mentioned by
dbSNPrs7115578
ebirs7115578
HLIrs7115578
Exacrs7115578
Varsomers7115578
Maprs7115578
PheGenIrs7115578
hapmaprs7115578
1000 genomesrs7115578
hgdprs7115578
ensemblrs7115578
gopubmedrs7115578
geneviewrs7115578
scholarrs7115578
googlers7115578
pharmgkbrs7115578
gwascentralrs7115578
openSNPrs7115578
23andMers7115578
23andMe allrs7115578
SNP Nexus

SNPshotrs7115578
SNPdbers7115578
MSV3drs7115578
GWAS Ctlgrs7115578
GMAF0.4265
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 A
P-val 0.000008
Odds Ratio 1.86 [1.23-2.79]




GET Evidence
rs7115578
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.4375
summary