Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10209110
AFF3
1.000 0.120 2 100056230 intron variant C/T snv 0.47 1
rs6712515
AFF3
0.925 0.160 2 100190052 intron variant T/A;C snv 1
rs11676922
AFF3
0.925 0.160 2 100190478 intron variant T/A snv 0.51 4
rs9653442
LINC01104
1.000 0.120 2 100208905 intron variant C/T snv 0.46 1
rs678347 1.000 0.120 8 101451374 intron variant G/A;C snv 1
rs646514 1.000 0.120 8 101453833 upstream gene variant C/G;T snv 1
rs17266594
BANK1
0.807 0.280 4 101829765 intron variant T/C snv 0.25 0.27 1
rs10516487
BANK1
0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 2
rs74956615
FDX2 ; RAVER1
0.807 0.160 19 10317045 3 prime UTR variant T/A;C snv 1
rs26232
MACIR
0.925 0.160 5 103261019 intron variant C/T snv 0.30 4
rs39984
MACIR
1.000 0.120 5 103261591 intron variant G/T snv 0.30 1
rs2561477
MACIR
1.000 0.120 5 103273223 intron variant G/A snv 0.24 1
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 4
rs2841277
PLD4
0.882 0.120 14 104924668 upstream gene variant C/T snv 0.41 1
rs2582532
PLD4
1.000 0.120 14 104926500 intron variant T/C snv 0.93 1
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 4
rs6568431
ATG5
0.790 0.320 6 106140931 intron variant A/C snv 0.61 2
rs9372120
ATG5
0.851 0.280 6 106219660 intron variant T/G snv 0.16 1
rs13142500
CLNK
1.000 0.120 4 10725733 intergenic variant T/C snv 0.43 1
rs1809529
SLC6A11
1.000 0.120 3 10835926 intron variant C/T snv 0.45 1
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 9
rs6732565
ACOXL
1.000 0.120 2 110850255 intron variant A/G snv 0.38 1
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 4
rs10774624
LINC02356
0.882 0.160 12 111395984 intron variant G/A snv 0.67 1
rs2903692
CLEC16A
0.807 0.360 16 11144926 intron variant G/A snv 0.33 1