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rs613120

From SNPedia

Orientationminus
Stabilizedminus
Make rs613120(C;C)
Make rs613120(C;T)
Make rs613120(T;T)
ReferenceGRCh38 38.1/141
Chromosome11
Position101103547
GenePGR
is asnp
is mentioned by
dbSNPrs613120
ebirs613120
HLIrs613120
Exacrs613120
Varsomers613120
Maprs613120
PheGenIrs613120
hapmaprs613120
1000 genomesrs613120
hgdprs613120
ensemblrs613120
gopubmedrs613120
geneviewrs613120
scholarrs613120
googlers613120
pharmgkbrs613120
gwascentralrs613120
openSNPrs613120
23andMers613120
23andMe allrs613120
SNP Nexus

SNPshotrs613120
SNPdbers613120
MSV3drs613120
GWAS Ctlgrs613120
Max Magnitude
Part of a haplotype Gs286, standalone effect for endometrial cancer is ambiguous.
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 0.52
Odds Ratio 1.05 [0.91-1.21]

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