Source: CLINVAR ×
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.
Fabry Disease
CUI: C0002986
Disease: Fabry Disease
135 1.000 0.160 X 101403845 missense variant C/A;T snv 1.1E-05 0.800 1.000 13 1989 2017