Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12979860
IFNL4
0.547 0.520 19 39248147 intron variant C/T snv 0.39 84
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs483352822
RIT1
0.776 0.360 1 155904470 stop lost C/A;G;T snv 16
rs104894809
GATA1
0.790 0.120 X 48792371 missense variant G/A snv 9.5E-06 9
rs483352867
STIM1
0.827 0.400 11 4074620 missense variant C/T snv 8
rs121912713
SERPINA1
0.851 0.200 14 94378561 missense variant A/C snv 5
rs886043118
STAT1
0.925 0.040 2 191009916 frameshift variant T/- delins 5
rs387907201
F2
1.000 0.080 11 46739326 missense variant G/A;T snv 4
rs1482856709
PROS1
0.925 0.080 3 93900887 missense variant G/A snv 3
rs61750610
VWF
0.925 0.080 12 6013630 missense variant G/T snv 3
rs387906691
TBXA2R
1.000 19 3595810 missense variant C/T snv 2
rs575627531
ABCA1
1.000 0.120 9 104814211 stop gained G/A snv 2
rs1339688889
AAAS
12 53315733 missense variant C/T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121909675
GGCX
1.000 0.080 2 85553045 missense variant A/C snv 4.0E-06 7.0E-06 2
rs758865890
F11-AS1 ; F11
4 186288592 missense variant T/C snv 4.0E-06 1
rs61749397
VWF
0.807 0.080 12 6019472 missense variant C/G;T snv 4.0E-06 9
rs1252993409
ADRA1A
8 26864323 missense variant C/T snv 4.0E-06 7.0E-06 1
rs780463965
LPAR2
19 19626638 missense variant C/A;T snv 4.0E-06; 1.6E-05 1
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs72547528
VKORC1 ; PRSS53
0.925 0.120 16 31091334 missense variant G/A;C snv 7.2E-05; 8.1E-06 3
rs757075712
TFAM
0.763 0.200 10 58390856 missense variant C/T snv 1.6E-05 1.4E-05 15
rs557043245
MED12L ; P2RY12
3 151338482 missense variant G/A snv 4.0E-05 7.0E-06 1
rs34377097
TBXA2R
1.000 19 3600456 missense variant C/A snv 5.8E-05 2.1E-05 2