rs3809060, WT1-AS;WT1

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 11 32437261 intron variant G/T snv 0.49 0.700 1.000 1 2019 2019
Hernia, Inguinal
CUI: C0019294
Disease: Hernia, Inguinal
21 11 32437261 intron variant G/T snv 0.49 0.700 1.000 1 2015 2015