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rs1879352

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common on affy axiom data
Make rs1879352(A;G)
Make rs1879352(G;G)
ReferenceGRCh38 38.1/142
Chromosome18
Position2498055
is asnp
is mentioned by
dbSNPrs1879352
ebirs1879352
HLIrs1879352
Exacrs1879352
Varsomers1879352
Maprs1879352
PheGenIrs1879352
hapmaprs1879352
1000 genomesrs1879352
hgdprs1879352
ensemblrs1879352
gopubmedrs1879352
geneviewrs1879352
scholarrs1879352
googlers1879352
pharmgkbrs1879352
gwascentralrs1879352
openSNPrs1879352
23andMers1879352
23andMe allrs1879352
SNP Nexus

SNPshotrs1879352
SNPdbers1879352
MSV3drs1879352
GWAS Ctlgrs1879352
GMAF0.09412
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 C
P-val 0.000009
Odds Ratio 1.53 [1.20-1.80]


GET Evidence
rs1879352
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.078125
summary