Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs786205050
CACNA1H
0.827 0.080 16 1212024 missense variant A/G snv 7.0E-06 7
rs760695410
WBP1L ; CYP17A1 ; CYP17A1-AS1
0.807 0.240 10 102832532 missense variant T/A snv 1.2E-05; 4.0E-06 6
rs6203
HSD3B1
0.851 0.120 1 119514535 synonymous variant C/T snv 0.45 0.35 4
rs12410453 0.925 0.040 1 119410216 upstream gene variant G/A snv 4.1E-03 2