rs1256061, ESR2

N. diseases: 5
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Red Blood Cell Count measurement
CUI: C0014772
Disease: Red Blood Cell Count measurement
1599 14 64236875 intron variant G/A;T snv 0.700 1.000 2 2016 2019
Corpuscular Hemoglobin Concentration Mean
CUI: C4528257
Disease: Corpuscular Hemoglobin Concentration Mean
4389 14 64236875 intron variant G/A;T snv 0.700 1.000 1 2012 2012
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 14 64236875 intron variant G/A;T snv 0.700 1.000 1 2016 2016
Hemoglobin measurement
CUI: C0518015
Disease: Hemoglobin measurement
224 14 64236875 intron variant G/A;T snv 0.700 1.000 1 2016 2016
Lung Neoplasms
CUI: C0024121
Disease: Lung Neoplasms
39 14 64236875 intron variant G/A;T snv 0.010 1.000 1 2013 2013