rs1185695012, WHRN

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.
Nonsyndromic Deafness
CUI: C3711374
Disease: Nonsyndromic Deafness
66 0.925 0.200 9 114403898 missense variant G/A snv 4.0E-06 0.010 1.000 1 2014 2014
Usher Syndrome, Type II
CUI: C1568249
Disease: Usher Syndrome, Type II
7 0.925 0.200 9 114403898 missense variant G/A snv 4.0E-06 0.010 1.000 1 2014 2014