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rs2277439

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2277439(A;A)
Make rs2277439(A;G)
ReferenceGRCh38 38.1/141
Chromosome13
Position42581307
GeneTNFSF11
is asnp
is mentioned by
dbSNPrs2277439
ebirs2277439
HLIrs2277439
Exacrs2277439
Varsomers2277439
Maprs2277439
PheGenIrs2277439
hapmaprs2277439
1000 genomesrs2277439
hgdprs2277439
ensemblrs2277439
gopubmedrs2277439
geneviewrs2277439
scholarrs2277439
googlers2277439
pharmgkbrs2277439
gwascentralrs2277439
openSNPrs2277439
23andMers2277439
23andMe allrs2277439
SNP Nexus

SNPshotrs2277439
SNPdbers2277439
MSV3drs2277439
GWAS Ctlgrs2277439
Max Magnitude0
? (A;A) (A;G) (G;G) 28

[PMID 25138264] Polymorphisms in genes in the RANKL/RANK/OPG pathway are associated with bone mineral density at different skeletal sites in post-menopausal women


ClinVar
Risk rs2277439(A;A)
Alt rs2277439(A;A)
Reference rs2277439(G;G)
Significance Non-pathogenic
Disease not specified
Variation info
Gene TNFSF11
CLNDBN not specified
Reversed 0
HGVS NC_000013.10:g.43155443G>A
CLNSRC
CLNACC RCV000175758.1,