rs2175898, ESR1

N. diseases: 2
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.
Cardiovascular Diseases
CUI: C0007222
Disease: Cardiovascular Diseases
711 6 151875817 intron variant C/G;T snv 0.010 1.000 1 2016 2016
Depressive Symptoms
CUI: C0086132
Disease: Depressive Symptoms
120 6 151875817 intron variant C/G;T snv 0.010 1.000 1 2016 2016