rs381949, CLPTM1L

N. diseases: 3
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 1.000 0.040 5 1322353 intron variant G/A snv 0.44 0.700 1.000 1 2018 2018
Lower Urinary Tract Symptoms
CUI: C0574785
Disease: Lower Urinary Tract Symptoms
30 1.000 0.040 5 1322353 intron variant G/A snv 0.44 0.700 1.000 1 2018 2018
Prostate specific antigen measurement
CUI: C0201544
Disease: Prostate specific antigen measurement
95 1.000 0.040 5 1322353 intron variant G/A snv 0.44 0.700 1.000 1 2018 2018