rs1564602202, MYO3A

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 Recessive 30
CUI: C1846784
Disease: Deafness, Autosomal Recessive 30
7 1.000 0.120 10 26153849 splice acceptor variant G/T snv 0.700 0
hearing impairment
CUI: C1384666
Disease: hearing impairment
337 1.000 0.120 10 26153849 splice acceptor variant G/T snv 0.700 0