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rs41322152

From SNPedia

Orientationplus
Stabilizedplus
Make rs41322152(C;C)
Make rs41322152(C;G)
Make rs41322152(G;G)
ReferenceGRCh38 38.1/142
Chromosome10
Position70281049
GeneNPFFR1
is asnp
is mentioned by
dbSNPrs41322152
ebirs41322152
HLIrs41322152
Exacrs41322152
Varsomers41322152
Maprs41322152
PheGenIrs41322152
hapmaprs41322152
1000 genomesrs41322152
hgdprs41322152
ensemblrs41322152
gopubmedrs41322152
geneviewrs41322152
scholarrs41322152
googlers41322152
pharmgkbrs41322152
gwascentralrs41322152
openSNPrs41322152
23andMers41322152
23andMe allrs41322152
SNP Nexus

SNPshotrs41322152
SNPdbers41322152
MSV3drs41322152
GWAS Ctlgrs41322152
GMAF0.02479
Max Magnitude
? (C;C) (C;G) (G;G) 28
GWAS snp
PMID [PMID 23007406OA-icon.png]
Trait Acute lymphoblastic leukemia (childhood)
Title Genome-wide association study identifies germline polymorphisms associated with relapse of childhood acute lymphoblastic leukemia.
Risk Allele C
P-val 8E-6
Odds Ratio 2.52 [1.68-3.79]