CLPTM1L, CLPTM1 like, 81037

N. diseases: 110; N. variants: 20
Disease: Benign Prostatic Hyperplasia ×
Source: ALL
Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs381949
rs381949 		1.000 0.040 5 1322353 intron variant G/A snv 0.44
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia 		Male Urogenital Diseases 0.700 1.000 1 2018 2018