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rs1569788

From SNPedia

Orientationplus
Stabilizedplus
Make rs1569788(C;C)
Make rs1569788(C;T)
Make rs1569788(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position152007481
GeneESR1
is asnp
is mentioned by
dbSNPrs1569788
ebirs1569788
HLIrs1569788
Exacrs1569788
Varsomers1569788
Maprs1569788
PheGenIrs1569788
hapmaprs1569788
1000 genomesrs1569788
hgdprs1569788
ensemblrs1569788
gopubmedrs1569788
geneviewrs1569788
scholarrs1569788
googlers1569788
pharmgkbrs1569788
gwascentralrs1569788
openSNPrs1569788
23andMers1569788
23andMe allrs1569788
SNP Nexus

SNPshotrs1569788
SNPdbers1569788
MSV3drs1569788
GWAS Ctlgrs1569788
GMAF0.4132
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 18305958OA-icon.png] 577 African American individuals with T2DM-ESRD and 596 AA controls.
  • rs1569788 (nominal P = 0.000754, adjusted P = 0.0278)


[PMID 20797716] Epistasis between CYP19A1 and ESR1 polymorphisms is associated with premature ovarian failure


[PMID 18654799OA-icon.png] Exploration of the utility of ancestry informative markers for genetic association studies of African Americans with type 2 diabetes and end stage renal disease.