rs8100454, CYP2F2P

N. diseases: 1
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 19 40820613 intron variant A/G snv 9.7E-02 0.700 1.000 1 2016 2016