Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs751377893
F5
0.574 0.680 1 169546513 missense variant T/C snv 4.0E-06 65
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 33
rs5918
ITGB3
0.683 0.480 17 47283364 missense variant T/C snv 0.12 0.13 26
rs2519093
ABO
0.882 0.200 9 133266456 intron variant T/C snv 16
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 16
rs121918474
PROS1
0.763 0.320 3 93905799 missense variant T/C snv 2.8E-05 1.4E-05 11
rs1312546120
F5
0.807 0.160 1 169541191 missense variant T/C snv 4.0E-06 7
rs114209171
FUNDC2
0.882 0.120 X 155050522 non coding transcript exon variant T/C snv 0.23 5
rs2036914
F11
0.882 0.160 4 186271327 intron variant T/C snv 0.57 5
rs633862 0.925 0.120 9 133279871 upstream gene variant T/C snv 0.49 5
rs710446
KNG1
0.925 0.120 3 186742138 missense variant T/C snv 0.42 0.44 4
rs12061601 1.000 0.040 1 169101212 intron variant T/C snv 0.16 3
rs4524
F5
1 169542517 missense variant T/C snv 0.28 0.24 3
rs574347
ABO
9 133260255 intron variant T/C snv 0.27 3
rs5758896
A4GALT
22 42719570 intron variant T/C snv 0.55 3
rs6825454 1.000 0.080 4 154580036 downstream gene variant T/C snv 0.25 3
rs77641731
ABO
1.000 0.040 9 133257521 missense variant T/C snv 3
rs8176681
ABO
9 133264351 intron variant T/C snv 3
rs9390460
STXBP5
6 147373198 intron variant T/C snv 0.51 3
rs10029715
F11-AS1
4 186301446 intron variant T/C snv 0.22 2
rs1042580
THBD
20 23046984 3 prime UTR variant T/C snv 0.33 2
rs12500826
F11-AS1
4 186306297 intron variant T/C snv 0.60 2
rs142846443
PROS1
1.000 0.120 3 93877074 missense variant T/C snv 8.0E-04 4.3E-04 2
rs78707713
TSPAN15
1.000 0.120 10 69485520 intron variant T/C snv 8.5E-02 2
rs10090114
MSRA
8 10147444 intron variant T/C snv 0.90 1