Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 13
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs6063514 0.776 0.080 20 50438781 intergenic variant C/T snv 0.42 11
rs77542162
ABCA6
1.000 0.040 17 69085137 missense variant A/G snv 9.3E-03 1.0E-02 11
rs2571445
TNS1
0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 10
rs8176693
ABO
0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 9
rs4656461 0.827 0.040 1 165717968 TF binding site variant G/A snv 0.85 7
rs8176743
ABO
1.000 0.040 9 133256028 missense variant C/T snv 0.12 0.11 7
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 7
rs202676
FOLH1
0.851 0.160 11 49206068 stop lost A/G snv 0.28 0.33 7
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 7
rs11024102
PLEKHA7
0.851 0.040 11 16987058 intron variant T/C snv 0.20 7
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 6
rs10774624
LINC02356
0.882 0.160 12 111395984 intron variant G/A snv 0.67 6
rs1042602
LOC107984363 ; TYR
0.925 0.080 11 89178528 missense variant C/A snv 0.25 0.24 6
rs72681869
SOS2
14 50188639 missense variant G/A;C snv 4.0E-06; 4.1E-03 6
rs28383314 0.925 0.160 6 32619436 regulatory region variant T/C snv 0.61 5
rs72755233
ADAMTS17
1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 5
rs11656696
GAS7
0.882 0.040 17 10130362 intron variant C/A snv 0.36 5
rs2472493
LOC105376196
0.851 0.040 9 104933567 downstream gene variant G/A snv 0.61 5
rs113542380
THADA
2 43237679 intron variant G/A snv 4.7E-02 5
rs4236601 0.882 0.040 7 116522675 upstream gene variant G/A snv 0.28 4
rs747782 0.925 0.040 11 47919373 intergenic variant T/C snv 0.26 4
rs9938149 0.925 0.160 16 88298034 intron variant C/A snv 0.66 4
rs5896
F2
0.882 0.160 11 46723453 missense variant C/G;T snv 0.21 4