Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs899127658
F2
0.547 0.720 11 46739084 missense variant G/A;C snv 82
rs1183194405
F2
0.716 0.440 11 46719773 missense variant G/A;T snv 4.5E-06; 4.5E-06 19
rs146922325
LOC105373608 ; PROC
0.851 0.160 2 127426114 missense variant C/T snv 7.5E-04 3.2E-04 5
rs121918146
PROC ; LOC105373608
0.827 0.200 2 127428485 missense variant G/A snv 1.2E-05 2.1E-05 5
rs121912713
SERPINA1
0.851 0.200 14 94378561 missense variant A/C snv 5
rs121918156
LOC105373608 ; PROC
0.882 0.120 2 127427219 missense variant C/T snv 3
rs121918143
PROC ; LOC105373608
0.882 0.080 2 127426180 missense variant C/A;T snv 4.0E-06; 2.8E-05 3
rs767730328
LOC105373608 ; PROC
0.925 0.080 2 127428660 missense variant T/C snv 4.0E-06 2
rs121918153
PROC ; LOC105373608
0.925 0.080 2 127426208 missense variant G/A;T snv 9.5E-05; 8.0E-06 2
rs142742242
PROC ; LOC105373608
0.925 0.080 2 127428761 missense variant G/A snv 3.2E-05 7.0E-06 2
rs121909552
SERPINC1
0.925 0.080 1 173914725 missense variant C/T snv 9.5E-05 1.7E-04 2
rs572021052
PROC ; LOC105373608
1.000 0.080 2 127428797 missense variant A/G snv 7.0E-06 1