Source: ALL

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: rs28935195
rs28935195
GLA ; RPL36A-HNRNPH2
0.925 0.200 X 101401713 missense variant C/T snv
CUI: C0002986
Disease: Fabry Disease
Fabry Disease 		0.810 1.000 31 1989 2017
dbSNP: rs28935195
rs28935195
GLA ; RPL36A-HNRNPH2
0.925 0.200 X 101401713 missense variant C/T snv
CUI: C0030591
Disease: Paroxysmal ventricular tachycardia
Paroxysmal ventricular tachycardia 		0.010 1.000 1 2010 2010