rs17882106
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs17882106(C;C) |
Make rs17882106(C;T) |
Make rs17882106(T;T) |
Reference | GRCh38.p7 38.3/149 |
Chromosome | 12 |
Position | 47900630 |
Gene | VDR |
is a | snp |
is | mentioned by |
dbSNP | rs17882106 |
dbSNP (classic) | rs17882106 |
ClinGen | rs17882106 |
ebi | rs17882106 |
HLI | rs17882106 |
Exac | rs17882106 |
Gnomad | rs17882106 |
Varsome | rs17882106 |
LitVar | rs17882106 |
Map | rs17882106 |
PheGenI | rs17882106 |
Biobank | rs17882106 |
1000 genomes | rs17882106 |
hgdp | rs17882106 |
ensembl | rs17882106 |
geneview | rs17882106 |
scholar | rs17882106 |
rs17882106 | |
pharmgkb | rs17882106 |
gwascentral | rs17882106 |
openSNP | rs17882106 |
23andMe | rs17882106 |
SNPshot | rs17882106 |
SNPdbe | rs17882106 |
MSV3d | rs17882106 |
GWAS Ctlg | rs17882106 |
Max Magnitude | 0 |
[PMID 28212442] Ecto-5' -Nucleotidase CD73 (NT5E), vitamin D receptor and FGF23 gene polymorphisms may play a role in the development of calcific uremic arteriolopathy in dialysis patients - Data from the German Calciphylaxis Registry.