rs78105154, ELAC2

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.
Benign Prostatic Hyperplasia
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
91 0.925 0.080 17 12994991 missense variant G/A snv 3.2E-04 7.0E-05 0.010 1.000 1 2003 2003
Prostate cancer, familial
CUI: C2931456
Disease: Prostate cancer, familial
25 0.925 0.080 17 12994991 missense variant G/A snv 3.2E-04 7.0E-05 0.010 1.000 1 2003 2003