rs1176235580, MTO1

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.
hearing impairment
CUI: C1384666
Disease: hearing impairment
337 0.925 0.120 6 73482214 missense variant G/A snv 0.010 1.000 1 2003 2003
Mitochondrial DNA mutation
CUI: C0948444
Disease: Mitochondrial DNA mutation
7 0.925 0.120 6 73482214 missense variant G/A snv 0.010 1.000 1 2003 2003
Sensorineural Hearing Loss (disorder)
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
111 0.925 0.120 6 73482214 missense variant G/A snv 0.010 1.000 1 2003 2003