rs768290597, ACTG2

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.
Visceral Myopathy
CUI: C0042781
Disease: Visceral Myopathy
19 1.000 0.040 2 73902698 missense variant C/A snv 9.8E-05 1.2E-04 0.700 0