Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv 6
rs2036914
F11
0.882 0.160 4 186271327 intron variant T/C snv 0.57 4
rs2227589
SERPINC1
0.925 0.120 1 173917078 intron variant C/T snv 9.6E-02 3
rs6507931
LIPG
0.882 0.080 18 49586638 intron variant C/T snv 0.52 3
rs2097055
LIPG
0.925 0.040 18 49569117 intron variant T/C snv 0.55 2
rs2227721
VTN ; SARM1
0.925 0.080 17 28370430 intron variant C/A;T snv 0.12 2
rs529565
ABO
0.851 0.120 9 133274084 intron variant C/T snv 2
rs12634349
PROS1
1.000 0.040 3 93882955 intron variant A/G snv 0.34 1
rs13062355
PROS1
1.000 0.040 3 93969667 intron variant G/A snv 0.46 1
rs422187
F9
1.000 0.040 X 139550700 intron variant A/C;G snv 1
rs6441600
PROS1
1.000 0.040 3 93956895 intron variant C/G snv 0.97 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1799983
NOS3
0.430 0.880 7 150999023 missense variant T/A;G snv 0.75 246
rs77375493
INSL6 ; JAK2
0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 181
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 169
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs1801394
FASTKD3 ; MTRR
0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 92
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
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 39
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 34