rs10521467, PCSK5

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.
Leukemia, Myelocytic, Acute
CUI: C0023467
Disease: Leukemia, Myelocytic, Acute
6892 0.925 0.080 9 76036575 intron variant A/G snv 0.12 0.700 1.000 1 2017 2017
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.925 0.080 9 76036575 intron variant A/G snv 0.12 0.010 1.000 1 2019 2019