rs587777692, P2RX2

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.
DEAFNESS, AUTOSOMAL DOMINANT 41 (disorder)
CUI: C1842371
Disease: DEAFNESS, AUTOSOMAL DOMINANT 41 (disorder)
2 0.925 0.120 12 132619443 missense variant G/T snv 0.800 1.000 2 2013 2014
Hearing Loss, High-Frequency
CUI: C0018780
Disease: Hearing Loss, High-Frequency
8 0.925 0.120 12 132619443 missense variant G/T snv 0.010 1.000 1 2013 2013