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rs3087869

From SNPedia

Orientationminus
Stabilizedminus
Make rs3087869(C;C)
Make rs3087869(C;T)
Make rs3087869(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position19953984
GeneCOMT
is asnp
is mentioned by
dbSNPrs3087869
ebirs3087869
HLIrs3087869
Exacrs3087869
Varsomers3087869
Maprs3087869
PheGenIrs3087869
hapmaprs3087869
1000 genomesrs3087869
hgdprs3087869
ensemblrs3087869
gopubmedrs3087869
geneviewrs3087869
scholarrs3087869
googlers3087869
pharmgkbrs3087869
gwascentralrs3087869
openSNPrs3087869
23andMers3087869
23andMe allrs3087869
SNP Nexus

SNPshotrs3087869
SNPdbers3087869
MSV3drs3087869
GWAS Ctlgrs3087869
GMAF0.4977
Max Magnitude

[PMID 24320736] Role of single nucleotide polymorphisms in estrogen-metabolizing enzymes and susceptibility to uterine leiomyoma in Han Chinese: A case-control study

[PMID 24777039] A Multicenter Case-Control Study on Screening of Single Nucleotide Polymorphisms in Estrogen-Metabolizing Enzymes and Susceptibility to Uterine Leiomyoma in Han Chinese