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rs4273077

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 1 Normal risk for development of MGUS
(A;G) 1 Possibly slight 1.09x risk for development of MGUS
(G;G) 2 3.57x increased risk of MGUS
ReferenceGRCh38 38.1/141
Chromosome17
Position16945825
GeneTNFRSF13B
is asnp
is mentioned by
dbSNPrs4273077
ebirs4273077
HLIrs4273077
Exacrs4273077
Varsomers4273077
Maprs4273077
PheGenIrs4273077
hapmaprs4273077
1000 genomesrs4273077
hgdprs4273077
ensemblrs4273077
gopubmedrs4273077
geneviewrs4273077
scholarrs4273077
googlers4273077
pharmgkbrs4273077
gwascentralrs4273077
openSNPrs4273077
23andMers4273077
23andMe allrs4273077
SNP Nexus

SNPshotrs4273077
SNPdbers4273077
MSV3drs4273077
GWAS Ctlgrs4273077
GMAF0.2176
Max Magnitude2
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 20139978]
Trait Hematological and biochemical traits
Title Genome-wide association study of hematological and biochemical traits in a Japanese population
Risk Allele G
P-val 3E-10
Odds Ratio 0.38 [NR] % variance


[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 G
P-val 8E-9
Odds Ratio 1.26 [1.16-1.36]