rs80358277, KCNQ4

N. diseases: 1
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 2A
CUI: C2677637
Disease: Deafness, Autosomal Dominant 2A
25 1.000 0.120 1 40819465 missense variant G/C snv 7.0E-06 0.800 1.000 5 1999 2011