rs797045898, POMT2

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.
Muscular Dystrophy
CUI: C0026850
Disease: Muscular Dystrophy
67 1.000 0.120 14 77283874 splice acceptor variant CTAGG/TCA delins 0.700 0