rs2280543

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in complete genomics
(C;T)

Make rs2280543(T;T)

Reference

GRCh37 37.1/132

Chromosome

11

Position

203788

Gene

BET1L

is a	snp
is	mentioned by
dbSNP	rs2280543
dbSNP (classic)	rs2280543
ClinGen	rs2280543
ebi	rs2280543
HLI	rs2280543
Exac	rs2280543
Gnomad	rs2280543
Varsome	rs2280543
LitVar	rs2280543
Map	rs2280543
PheGenI	rs2280543
Biobank	rs2280543
1000 genomes	rs2280543
hgdp	rs2280543
ensembl	rs2280543
geneview	rs2280543
scholar	rs2280543
google	rs2280543
pharmgkb	rs2280543
gwascentral	rs2280543
openSNP	rs2280543
23andMe	rs2280543
SNPshot	rs2280543
SNPdbe	rs2280543
MSV3d	rs2280543
GWAS Ctlg	rs2280543

GMAF

0.06979

Max Magnitude

0

?	(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 23604678] BET1L and TNRC6B associate with uterine fibroid risk among European Americans

[PMID 23892540] Variants in BET1L and TNRC6B associate with increasing fibroid volume and fibroid type among European Americans