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: rs3797177
rs3797177
1.000 0.040 5 6666971 intron variant T/A;C snv
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia
Male Urogenital Diseases 0.010 1.000 1 2017 2017
dbSNP: rs6884552
rs6884552
1.000 0.040 5 6661853 intron variant C/T snv 0.32
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia
Male Urogenital Diseases 0.010 1.000 1 2017 2017