rs2502992
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs2502992(A;A) |
Make rs2502992(A;G) |
Make rs2502992(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 1 |
Position | 23875429 |
Gene | CNR2 |
is a | snp |
is | mentioned by |
dbSNP | rs2502992 |
dbSNP (classic) | rs2502992 |
ClinGen | rs2502992 |
ebi | rs2502992 |
HLI | rs2502992 |
Exac | rs2502992 |
Gnomad | rs2502992 |
Varsome | rs2502992 |
LitVar | rs2502992 |
Map | rs2502992 |
PheGenI | rs2502992 |
Biobank | rs2502992 |
1000 genomes | rs2502992 |
hgdp | rs2502992 |
ensembl | rs2502992 |
geneview | rs2502992 |
scholar | rs2502992 |
rs2502992 | |
pharmgkb | rs2502992 |
gwascentral | rs2502992 |
openSNP | rs2502992 |
23andMe | rs2502992 |
SNPshot | rs2502992 |
SNPdbe | rs2502992 |
MSV3d | rs2502992 |
GWAS Ctlg | rs2502992 |
Max Magnitude | 0 |
[PMID 26055357] Evaluation of common variants in CNR2 gene for bone mineral density and osteoporosis susceptibility in postmenopausal women of Han Chinese