Have questions? Visit https://www.reddit.com/r/SNPedia

rs2172873

From SNPedia

Orientationminus
Stabilizedminus
Make rs2172873(C;C)
Make rs2172873(C;T)
Make rs2172873(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position102731912
is asnp
is mentioned by
dbSNPrs2172873
ebirs2172873
HLIrs2172873
Exacrs2172873
Varsomers2172873
Maprs2172873
PheGenIrs2172873
hapmaprs2172873
1000 genomesrs2172873
hgdprs2172873
ensemblrs2172873
gopubmedrs2172873
geneviewrs2172873
scholarrs2172873
googlers2172873
pharmgkbrs2172873
gwascentralrs2172873
openSNPrs2172873
23andMers2172873
23andMe allrs2172873
SNP Nexus

SNPshotrs2172873
SNPdbers2172873
MSV3drs2172873
GWAS Ctlgrs2172873
GMAF0.1327
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21460842]
Trait
Title A genome-wide association study identifies three loci associated with susceptibility to uterine fibroids
Risk Allele A
P-val 0.000002
Odds Ratio 1.1800 [1.04-1.34]