Have questions? Visit https://www.reddit.com/r/SNPedia

rs877529

From SNPedia

Orientationminus
Stabilizedminus
Make rs877529(C;C)
Make rs877529(C;T)
Make rs877529(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position39146287
GeneCBX7
is asnp
is mentioned by
dbSNPrs877529
ebirs877529
HLIrs877529
Exacrs877529
Varsomers877529
Maprs877529
PheGenIrs877529
hapmaprs877529
1000 genomesrs877529
hgdprs877529
ensemblrs877529
gopubmedrs877529
geneviewrs877529
scholarrs877529
googlers877529
pharmgkbrs877529
gwascentralrs877529
openSNPrs877529
23andMers877529
23andMe allrs877529
SNP Nexus

SNPshotrs877529
SNPdbers877529
MSV3drs877529
GWAS Ctlgrs877529
GMAF0.3444
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 24449210] Inherited genetic susceptibility to monoclonal gammopathy of unknown significance

GWAS snp
PMID [PMID 23955597]
Trait Multiple myeloma
Title Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk.
Risk Allele A
P-val 8E-16
Odds Ratio 1.23 [1.17-1.29]