rs144446375, CEMIP

N. diseases: 2
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 1.000 0.120 15 80881079 missense variant G/A snv 1.2E-05 4.2E-05 0.010 1 2003 2003
Nonsyndromic Deafness
CUI: C3711374
Disease: Nonsyndromic Deafness
66 1.000 0.120 15 80881079 missense variant G/A snv 1.2E-05 4.2E-05 0.010 1.000 1 2003 2003