Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8176693
ABO
0.851 0.160 9 133262254 intron variant C/T snv 9.9E-02 5
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 5
rs8176743
ABO
1.000 0.040 9 133256028 missense variant C/T snv 0.12 0.11 3
rs2571445
TNS1
0.925 0.080 2 217818431 missense variant A/G;T snv 0.62 3
rs3134954
TNXB
0.882 0.240 6 32104116 intron variant C/T snv 0.90 3
rs4656461 0.827 0.040 1 165717968 TF binding site variant G/A snv 0.85 2
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 2
rs7759938
LIN28B-AS1
0.925 0.120 6 104931079 intron variant C/T snv 0.62 2
rs1042602
LOC107984363 ; TYR
0.925 0.080 11 89178528 missense variant C/A snv 0.25 0.24 2
rs181362
UBE2L3
22 21577779 intron variant C/T snv 0.31 2
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 1
rs11616662 13 40545329 intron variant G/A snv 0.11 1
rs2721051 1.000 0.040 13 40536747 intron variant C/T snv 8.6E-02 1
rs28383314 0.925 0.160 6 32619436 regulatory region variant T/C snv 0.61 1
rs4236601 0.882 0.040 7 116522675 upstream gene variant G/A snv 0.28 1
rs59072263 7 8112437 upstream gene variant G/T snv 0.15 1
rs747782 0.925 0.040 11 47919373 intergenic variant T/C snv 0.26 1
rs9938149 0.925 0.160 16 88298034 intron variant C/A snv 0.66 1
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 1
rs1361108
CENPW
6 126446454 intron variant C/T snv 0.44 1
rs6445055
FNDC3B
0.925 0.040 3 172274597 intron variant G/A snv 0.24 1
rs202676
FOLH1
0.851 0.160 11 49206068 stop lost A/G snv 0.28 0.33 1
rs11656696
GAS7
0.882 0.040 17 10130362 intron variant C/A snv 0.36 1
rs12150284
GAS7
1.000 0.040 17 10127773 intron variant C/A;G;T snv 1
rs9913911
GAS7
0.925 0.040 17 10127866 intron variant A/G snv 0.32 1