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

rs10849033

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs10849033(A;G)
Make rs10849033(G;G)
ReferenceGRCh38 38.1/141
Chromosome12
Position4315956
is asnp
is mentioned by
dbSNPrs10849033
ebirs10849033
HLIrs10849033
Exacrs10849033
Varsomers10849033
Maprs10849033
PheGenIrs10849033
hapmaprs10849033
1000 genomesrs10849033
hgdprs10849033
ensemblrs10849033
gopubmedrs10849033
geneviewrs10849033
scholarrs10849033
googlers10849033
pharmgkbrs10849033
gwascentralrs10849033
openSNPrs10849033
23andMers10849033
23andMe allrs10849033
SNP Nexus

SNPshotrs10849033
SNPdbers10849033
MSV3drs10849033
GWAS Ctlgrs10849033
GMAF0.2649
Max Magnitude0
? (A;A) (A;G) (G;G) 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 G
P-val 0.000009
Odds Ratio 2.55 [1.60-3.80]


GET Evidence
rs10849033
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.742188
summary