rs780027419, POU3F4

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.
Progressive hearing loss stapes fixation
35 1.000 0.160 X 83509201 missense variant C/G;T snv 5.5E-06 0.700 0
X- linked recessive
CUI: C1845977
Disease: X- linked recessive
1 1.000 0.160 X 83509201 missense variant C/G;T snv 5.5E-06 0.700 0