Source: CURATED ×
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.
Myopathy
CUI: C0026848
Disease: Myopathy
74 10 132440647 intron variant T/C;G snv 0.700 1.000 1 2019 2019