rs2107301
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | normal risk |
(C;T) | ? | |
(T;T) | 3 | 2.5x higher risk for prostate cancer |
Reference | GRCh38 38.1/141 |
Chromosome | 12 |
Position | 47861787 |
Gene | VDR |
is a | snp |
is | mentioned by |
dbSNP | rs2107301 |
dbSNP (classic) | rs2107301 |
ClinGen | rs2107301 |
ebi | rs2107301 |
HLI | rs2107301 |
Exac | rs2107301 |
Gnomad | rs2107301 |
Varsome | rs2107301 |
LitVar | rs2107301 |
Map | rs2107301 |
PheGenI | rs2107301 |
Biobank | rs2107301 |
1000 genomes | rs2107301 |
hgdp | rs2107301 |
ensembl | rs2107301 |
geneview | rs2107301 |
scholar | rs2107301 |
rs2107301 | |
pharmgkb | rs2107301 |
gwascentral | rs2107301 |
openSNP | rs2107301 |
23andMe | rs2107301 |
SNPshot | rs2107301 |
SNPdbe | rs2107301 |
MSV3d | rs2107301 |
GWAS Ctlg | rs2107301 |
GMAF | 0.3572 |
Max Magnitude | 3 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
rs2107301 is a SNP in the vitamin D VDR receptor gene.
rs2107301(T;T) homozygotes were associated with an ~2.5x higher risk of prostate cancer compared to homozygote carriers of the more common (C) allele in the 630 Caucasian patients studied.[PMID 17932346]
[PMID 19255064] Vitamin D-related genes, serum vitamin D concentrations and prostate cancer risk.
[PMID 19454612] Vitamin D pathway gene variants and prostate cancer risk.
[PMID 19753122] Analysis of SNPs and haplotypes in vitamin D pathway genes and renal cancer risk.
[PMID 19956101] Overview of the Rapid Response data.
[PMID 21948293] Vitamin D Receptor Gene Variants and Esophageal Adenocarcinoma Risk: A Population-Based Case-Control Study.
[PMID 22576141] No association of vitamin D metabolism-related polymorphisms and melanoma risk as well as melanoma prognosis: a case-control study.
[PMID 24381141] Vitamin D receptor gene polymorphisms and esophageal cancer risk in a Chinese population: a negative study
[PMID 27736940] Vitamin D Receptor Gene Polymorphism and the Risk of Colorectal Cancer: A Nested Case-Control Study.