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rs3847987

From SNPedia

Orientationplus
Stabilizedplus
Make rs3847987(A;A)
Make rs3847987(A;C)
Make rs3847987(C;C)
ReferenceGRCh38 38.1/141
Chromosome12
Position47844285
GeneVDR
is asnp
is mentioned by
dbSNPrs3847987
ebirs3847987
HLIrs3847987
Exacrs3847987
Varsomers3847987
Maprs3847987
PheGenIrs3847987
hapmaprs3847987
1000 genomesrs3847987
hgdprs3847987
ensemblrs3847987
gopubmedrs3847987
geneviewrs3847987
scholarrs3847987
googlers3847987
pharmgkbrs3847987
gwascentralrs3847987
openSNPrs3847987
23andMers3847987
23andMe allrs3847987
SNP Nexus

SNPshotrs3847987
SNPdbers3847987
MSV3drs3847987
GWAS Ctlgrs3847987
GMAF0.1478
Max Magnitude
? (A;A) (A;C) (C;C) 28
rs3847987 in the vitamin D pathway was associated with the time to onset of COPD. The SNP is a cytosine-to-adenine switch, and men with two copies of the adenine variant were more likely to develop COPD. The hazard ratio was 1.60, with a 95% confidence interval from 1.26 to 2.05, which was significant at P=0.005. news


[PMID 17130574] Protection from type 1 diabetes by vitamin D receptor haplotypes.


[PMID 18593774OA-icon.png] Genetic and environmental determinants of 25-hydroxyvitamin D and 1,25-dihydroxyvitamin D levels in Hispanic and African Americans.


[PMID 27736940] Vitamin D Receptor Gene Polymorphism and the Risk of Colorectal Cancer: A Nested Case-Control Study.