rs145913750, TMPRSS3

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.
hearing impairment
CUI: C1384666
Disease: hearing impairment
337 21 42383169 missense variant G/A snv 2.4E-05 2.1E-05 0.010 1.000 1 2007 2007