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rs1870019

From SNPedia

Orientationminus
Stabilizedplus
Make rs1870019(C;C)
Make rs1870019(C;T)
Make rs1870019(T;T)
ReferenceGRCh38 38.1/142
Chromosome11
Position101030742
GenePGR
is asnp
is mentioned by
dbSNPrs1870019
ebirs1870019
HLIrs1870019
Exacrs1870019
Varsomers1870019
Maprs1870019
PheGenIrs1870019
hapmaprs1870019
1000 genomesrs1870019
hgdprs1870019
ensemblrs1870019
gopubmedrs1870019
geneviewrs1870019
scholarrs1870019
googlers1870019
pharmgkbrs1870019
gwascentralrs1870019
openSNPrs1870019
23andMers1870019
23andMe allrs1870019
SNP Nexus

SNPshotrs1870019
SNPdbers1870019
MSV3drs1870019
GWAS Ctlgrs1870019
Max Magnitude
? (C;C) (C;T) (T;T) 28
Part of a haplotype Gs286, standalone effect for endometrial cancer and ovarian cancer is ambiguous. p-values account for ethnic heterogenity of study population.
GWAS snp
PMID [PMID 20547493OA-icon.png]
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 0.74
Odds Ratio 0.91 [0.77-1.08]

[PMID 15632380] Clarifying the PROGINS allele association in ovarian and breast cancer risk: a haplotype-based analysis