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rs4795519

From SNPedia

Orientationplus
Stabilizedplus
Make rs4795519(A;A)
Make rs4795519(A;C)
Make rs4795519(C;C)
ReferenceGRCh38 38.1/141
Chromosome17
Position27214252
is asnp
is mentioned by
dbSNPrs4795519
ebirs4795519
HLIrs4795519
Exacrs4795519
Varsomers4795519
Maprs4795519
PheGenIrs4795519
hapmaprs4795519
1000 genomesrs4795519
hgdprs4795519
ensemblrs4795519
gopubmedrs4795519
geneviewrs4795519
scholarrs4795519
googlers4795519
pharmgkbrs4795519
gwascentralrs4795519
openSNPrs4795519
23andMers4795519
23andMe allrs4795519
SNP Nexus

SNPshotrs4795519
SNPdbers4795519
MSV3drs4795519
GWAS Ctlgrs4795519
GMAF0.4399
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 21540461]
Trait
Title A genome-wide association study identifies novel loci associated with susceptibility to chronic myeloid leukemia.
Risk Allele C
P-val 1E-12
Odds Ratio 1.8500 [1.56-2.17]