rs10140457
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10140457(A;A) |
Make rs10140457(A;C) |
Make rs10140457(C;C) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 14 |
Position | 64249975 |
Gene | ESR2 |
is a | snp |
is | mentioned by |
dbSNP | rs10140457 |
dbSNP (classic) | rs10140457 |
ClinGen | rs10140457 |
ebi | rs10140457 |
HLI | rs10140457 |
Exac | rs10140457 |
Gnomad | rs10140457 |
Varsome | rs10140457 |
LitVar | rs10140457 |
Map | rs10140457 |
PheGenI | rs10140457 |
Biobank | rs10140457 |
1000 genomes | rs10140457 |
hgdp | rs10140457 |
ensembl | rs10140457 |
geneview | rs10140457 |
scholar | rs10140457 |
rs10140457 | |
pharmgkb | rs10140457 |
gwascentral | rs10140457 |
openSNP | rs10140457 |
23andMe | rs10140457 |
SNPshot | rs10140457 |
SNPdbe | rs10140457 |
MSV3d | rs10140457 |
GWAS Ctlg | rs10140457 |
Max Magnitude | 0 |
[PMID 26536870] Associations between genetic variants and the effect of letrozole and exemestane on bone mass and bone turnover