rs7864987
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs7864987(C;C) |
Make rs7864987(C;T) |
Make rs7864987(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 9 |
Position | 134356320 |
Gene | RXRA |
is a | snp |
is | mentioned by |
dbSNP | rs7864987 |
dbSNP (classic) | rs7864987 |
ClinGen | rs7864987 |
ebi | rs7864987 |
HLI | rs7864987 |
Exac | rs7864987 |
Gnomad | rs7864987 |
Varsome | rs7864987 |
LitVar | rs7864987 |
Map | rs7864987 |
PheGenI | rs7864987 |
Biobank | rs7864987 |
1000 genomes | rs7864987 |
hgdp | rs7864987 |
ensembl | rs7864987 |
geneview | rs7864987 |
scholar | rs7864987 |
rs7864987 | |
pharmgkb | rs7864987 |
gwascentral | rs7864987 |
openSNP | rs7864987 |
23andMe | rs7864987 |
SNPshot | rs7864987 |
SNPdbe | rs7864987 |
MSV3d | rs7864987 |
GWAS Ctlg | rs7864987 |
GMAF | 0.2925 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23180655] Genetic variants in the vitamin D pathway and breast cancer disease-free survival