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
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 157
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs763780
IL17F
0.531 0.720 6 52236941 missense variant T/C snv 6.7E-02 6.6E-02 87
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
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs2397084
IL17F
0.716 0.480 6 52237046 missense variant T/C snv 6.7E-02 6.1E-02 14
rs11171806
IL23A
0.807 0.360 12 56339747 synonymous variant G/A snv 4.9E-02 4.5E-02 7
rs141012637
SERPINB10 ; SERPINB2
0.851 0.320 18 63901881 stop gained C/A;T snv 7.0E-05 4
rs398124629
APOH
0.925 0.120 17 66228149 missense variant T/C snv 2
rs764734814
PRR4 ; PRH1-PRR4 ; PRH2 ; PRH1
0.925 0.120 12 10930676 missense variant G/A snv 2.0E-05 7.0E-06 2
rs781289974
PROCR ; MMP24-AS1-EDEM2
1.000 0.120 20 35176773 missense variant C/T snv 4.0E-06 7.0E-06 1
rs1363677860
TP63
1.000 0.120 3 189864335 missense variant T/C snv 4.0E-06 1