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rs2302777

From SNPedia

Orientationplus
Stabilizedplus
Make rs2302777(A;A)
Make rs2302777(A;G)
Make rs2302777(G;G)
ReferenceGRCh38 38.1/141
Chromosome17
Position40023239
GeneMED24
is asnp
is mentioned by
dbSNPrs2302777
ebirs2302777
HLIrs2302777
Exacrs2302777
Varsomers2302777
Maprs2302777
PheGenIrs2302777
hapmaprs2302777
1000 genomesrs2302777
hgdprs2302777
ensemblrs2302777
gopubmedrs2302777
geneviewrs2302777
scholarrs2302777
googlers2302777
pharmgkbrs2302777
gwascentralrs2302777
openSNPrs2302777
23andMers2302777
23andMe allrs2302777
SNP Nexus

SNPshotrs2302777
SNPdbers2302777
MSV3drs2302777
GWAS Ctlgrs2302777
GMAF0.3159
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 23502783]
Trait Multiple myeloma (hyperdiploidy)
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-7
Odds Ratio 1.31 [1.18-1.46]


[PMID 27163155] Polymorphisms and Haplotypes of the Chromosome Locus 17q12-17q21.1 Contribute to Adult Asthma Susceptibility in Slovenian Patients.