UNC13A, unc-13 homolog A, 23025

N. diseases: 41; N. variants: 3
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: rs4239633
rs4239633 		0.851 0.240 19 17631660 intron variant C/T snv 0.32
CUI: C1704272
Disease: Benign Prostatic Hyperplasia
Benign Prostatic Hyperplasia 		Male Urogenital Diseases 0.700 1.000 1 2019 2019