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rs1994816

From SNPedia

Orientationplus
Stabilizedplus
Make rs1994816(A;A)
Make rs1994816(A;G)
Make rs1994816(G;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position180047278
is asnp
is mentioned by
dbSNPrs1994816
ebirs1994816
HLIrs1994816
Exacrs1994816
Varsomers1994816
Maprs1994816
PheGenIrs1994816
hapmaprs1994816
1000 genomesrs1994816
hgdprs1994816
ensemblrs1994816
gopubmedrs1994816
geneviewrs1994816
scholarrs1994816
googlers1994816
pharmgkbrs1994816
gwascentralrs1994816
openSNPrs1994816
23andMers1994816
23andMe allrs1994816
SNP Nexus

SNPshotrs1994816
SNPdbers1994816
MSV3drs1994816
GWAS Ctlgrs1994816
GMAF0.2782
Max Magnitude
? (A;A) (A;G) (G;G) 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 5E-7
Odds Ratio 1.76 [1.41-2.20]