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
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs1799963
F2
0.695 0.400 11 46739505 3 prime UTR variant G/A snv 9.6E-03 25
rs552953108
F2
0.724 0.200 11 46729529 missense variant G/A snv 1.6E-05 4.2E-05 16
rs368927897
JAK2 ; INSL6
0.790 0.240 9 5072541 missense variant G/A;T snv 2.8E-05; 6.4E-05 9
rs387906674
PROS1
0.925 0.040 3 93893025 missense variant G/A snv 2.0E-05 2
rs6123
PROS1
0.925 0.080 3 93874275 synonymous variant T/C snv 0.43 0.34 2
rs963668412
PROS1
0.925 0.040 3 93927362 missense variant C/T snv 8.0E-06 1.4E-05 2
rs1328295730
PROS1
1.000 0.040 3 93906074 missense variant G/A snv 1
rs753950548
PROS1
1.000 0.040 3 93910654 missense variant G/T snv 1.4E-05 1
rs1022228924
SHBG
1.000 0.040 17 7630506 missense variant A/G snv 1