rs28940306, MYH14

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 4
CUI: C1833503
Disease: Deafness, Autosomal Dominant 4
6 1.000 0.120 19 50271424 missense variant C/T snv 4.3E-06; 8.6E-06 0.800 1.000 2 2004 2005