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rs9290663

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common/normal
Make rs9290663(A;T)
Make rs9290663(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position178712151
GeneKCNMB2
is asnp
is mentioned by
dbSNPrs9290663
ebirs9290663
HLIrs9290663
Exacrs9290663
Varsomers9290663
Maprs9290663
PheGenIrs9290663
hapmaprs9290663
1000 genomesrs9290663
hgdprs9290663
ensemblrs9290663
gopubmedrs9290663
geneviewrs9290663
scholarrs9290663
googlers9290663
pharmgkbrs9290663
gwascentralrs9290663
openSNPrs9290663
23andMers9290663
23andMe allrs9290663
SNP Nexus

SNPshotrs9290663
SNPdbers9290663
MSV3drs9290663
GWAS Ctlgrs9290663
GMAF0.2144
Max Magnitude0
? (A;A) (A;T) (T;T) 28
GWAS snp
PMID [PMID 19684603OA-icon.png]
Trait Acute lymphoblastic leukemia (childhood)
Title Germline genomic variants associated with childhood acute lymphoblastic leukemia
Risk Allele T
P-val 0.000006
Odds Ratio 1.58 [1.20-1.90]


GET Evidence
rs9290663
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.3125
summary



[PMID 26177813] Replication analysis confirms the association of several variants with acute myeloid leukemia in Chinese population