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rs1449572

From SNPedia

Orientationminus
Stabilizedminus
Make rs1449572(A;A)
Make rs1449572(A;C)
Make rs1449572(C;C)
ReferenceGRCh38 38.1/141
Chromosome13
Position48892795
is asnp
is mentioned by
dbSNPrs1449572
ebirs1449572
HLIrs1449572
Exacrs1449572
Varsomers1449572
Maprs1449572
PheGenIrs1449572
hapmaprs1449572
1000 genomesrs1449572
hgdprs1449572
ensemblrs1449572
gopubmedrs1449572
geneviewrs1449572
scholarrs1449572
googlers1449572
pharmgkbrs1449572
gwascentralrs1449572
openSNPrs1449572
23andMers1449572
23andMe allrs1449572
SNP Nexus

SNPshotrs1449572
SNPdbers1449572
MSV3drs1449572
GWAS Ctlgrs1449572
GMAF0.1882
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 23502783]
Trait Multiple myeloma (IgH translocation)
Title The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma.
Risk Allele A
P-val 8E-6
Odds Ratio 1.73 [1.36-2.21]