Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs76428106
FLT3
0.851 0.040 13 28029870 intron variant T/C;G snv 10
rs11622435
LOC101928462
0.827 0.120 14 81151652 intron variant G/A snv 4.7E-02 7
rs2030519
LPP
0.827 0.200 3 188402113 intron variant G/A snv 0.61 7
rs3765209
LOC101927745
0.851 0.040 21 15417030 intron variant C/T snv 0.31 7
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv 7
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15 7
rs229541
C1QTNF6
0.807 0.200 22 37195278 intron variant G/A snv 0.49 6
rs3807307
IRF5
0.827 0.120 7 128939148 intron variant T/C snv 0.41 6
rs1032129
TNFRSF11B
0.851 0.040 8 118939661 intron variant A/C snv 0.37 5
rs11073337
RASGRP1
0.851 0.040 15 38555562 intron variant A/C snv 0.27 5
rs114378220
CAMK4
0.851 0.040 5 111230662 intron variant C/T snv 4.5E-02 5
rs11675342
TPO
0.851 0.040 2 1403856 intron variant C/T snv 0.40 5
rs11757201 0.851 0.040 6 137682685 intron variant G/C;T snv 5
rs12482947
UBASH3A
0.851 0.040 21 42431928 intron variant T/C snv 0.57 5
rs1443438
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv 5
rs1534430
MIR3681HG
0.851 0.040 2 12504610 intron variant C/T snv 0.35 5
rs2075302
FAP
0.882 2 162219636 intron variant T/C snv 0.34 5
rs5754100
UBE2L3
0.882 22 21561877 intron variant T/C snv 0.18 5
rs7441808
LINC02357
0.851 0.040 4 26088753 intron variant A/G snv 0.20 5
rs7568275
STAT4
0.827 0.120 2 191101726 intron variant G/C;T snv 5
rs761357
LINC00271
0.851 0.040 6 135581461 intron variant A/G;T snv 5
rs9507287
SPATA13
0.851 0.040 13 24212439 intron variant T/C snv 0.24 5
rs9591325
DLEU1
0.851 0.080 13 50237084 intron variant T/C snv 6.0E-02 5
rs10494079
VAV3
0.882 1 107832253 intron variant G/C snv 9.0E-02 4