Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs63749869
rs63749869
0.925 0.120 19 38580440 missense variant G/A snv
CUI: C0751951
Disease: Central Core Myopathy (disorder)
Central Core Myopathy (disorder)
0.710 1.000 2 2012 2018
dbSNP: rs63749869
rs63749869
0.925 0.120 19 38580440 missense variant G/A snv
Malignant hyperthermia susceptibility type 1
0.700 1.000 4 2004 2017