rs11039436, None

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.
Hematocrit procedure
CUI: C0018935
Disease: Hematocrit procedure
216 11 47866484 intergenic variant A/C;G;T snv 0.700 1.000 1 2016 2016
White Blood Cell Count procedure
CUI: C0023508
Disease: White Blood Cell Count procedure
1322 11 47866484 intergenic variant A/C;G;T snv 0.700 1.000 1 2016 2016