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: rs5516
rs5516
KLK1
0.827 0.120 19 50820217 missense variant C/G snv 0.69 0.67
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2007 2007
dbSNP: rs5517
rs5517
KLK1
1.000 0.040 19 50819976 missense variant T/C;G snv 0.33
CUI: C0020538
Disease: Hypertensive disease
Hypertensive disease 		0.010 1.000 1 2007 2007