rs373341, UBR2

N. diseases: 1
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.
Oligospermia
CUI: C0028960
Disease: Oligospermia
72 1.000 0.040 6 42691014 intron variant T/C;G snv 0.49; 5.2E-05 0.010 1.000 1 2016 2016