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rs2280543

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
(C;T)
Make rs2280543(T;T)
ReferenceGRCh37 37.1/132
Chromosome11
Position203788
GeneBET1L
is asnp
is mentioned by
dbSNPrs2280543
ebirs2280543
HLIrs2280543
Exacrs2280543
Varsomers2280543
Maprs2280543
PheGenIrs2280543
hapmaprs2280543
1000 genomesrs2280543
hgdprs2280543
ensemblrs2280543
gopubmedrs2280543
geneviewrs2280543
scholarrs2280543
googlers2280543
pharmgkbrs2280543
gwascentralrs2280543
openSNPrs2280543
23andMers2280543
23andMe allrs2280543
SNP Nexus

SNPshotrs2280543
SNPdbers2280543
MSV3drs2280543
GWAS Ctlgrs2280543
GMAF0.06979
Max Magnitude0
? (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 G
P-val 4E-12
Odds Ratio 1.3900 [1.17-1.64]
GWAS snp
PMID [PMID 22286173]
Trait
Title Genome-wide association study for intracranial aneurysm in the Japanese population identifies three candidate susceptible loci and a functional genetic variant at EDNRA.
Risk Allele T
P-val 0.000003
Odds Ratio 1.2510 None


[PMID 23604678OA-icon.png] BET1L and TNRC6B associate with uterine fibroid risk among European Americans


[PMID 23892540OA-icon.png] Variants in BET1L and TNRC6B associate with increasing fibroid volume and fibroid type among European Americans