rs543215
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs543215(A;A) |
Make rs543215(A;G) |
Make rs543215(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 101103302 |
Gene | PGR |
is a | snp |
is | mentioned by |
dbSNP | rs543215 |
dbSNP (classic) | rs543215 |
ClinGen | rs543215 |
ebi | rs543215 |
HLI | rs543215 |
Exac | rs543215 |
Gnomad | rs543215 |
Varsome | rs543215 |
LitVar | rs543215 |
Map | rs543215 |
PheGenI | rs543215 |
Biobank | rs543215 |
1000 genomes | rs543215 |
hgdp | rs543215 |
ensembl | rs543215 |
geneview | rs543215 |
scholar | rs543215 |
rs543215 | |
pharmgkb | rs543215 |
gwascentral | rs543215 |
openSNP | rs543215 |
23andMe | rs543215 |
SNPshot | rs543215 |
SNPdbe | rs543215 |
MSV3d | rs543215 |
GWAS Ctlg | rs543215 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
Part of a haplotype Gs286, standalone effect for endometrial cancer is ambiguous.
GWAS snp | |
---|---|
PMID | [PMID 20547493] |
Trait | Endometrial cancer |
Title | Genetic variation in the progesterone receptor gene and risk of endometrial cancer: a haplotype-based approach. |
Risk Allele | G |
P-val | 0.65 |
Odds Ratio | 1.12 [0.95-1.33] |
[PMID 15632380] Clarifying the PROGINS allele association in ovarian and breast cancer risk: a haplotype-based analysis