rs387906931, WFS1

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.
Wolfram-Like Syndrome, Autosomal Dominant
CUI: C3280358
Disease: Wolfram-Like Syndrome, Autosomal Dominant
5 0.925 0.360 4 6302133 missense variant G/A snv 0.800 1.000 3 2006 2011
Sensorineural Hearing Loss (disorder)
CUI: C0018784
Disease: Sensorineural Hearing Loss (disorder)
111 0.925 0.360 4 6302133 missense variant G/A snv 0.010 1.000 1 2011 2011