Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs10494079
VAV3
0.882 1 107832253 intron variant G/C snv 9.0E-02 4
rs5754100
UBE2L3
0.882 22 21561877 intron variant T/C snv 0.18 5
rs12482947
UBASH3A
0.851 0.040 21 42431928 intron variant T/C snv 0.57 5
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 20
rs11675342
TPO
0.851 0.040 2 1403856 intron variant C/T snv 0.40 5
rs4246905
TNFSF15
0.716 0.400 9 114790969 missense variant T/A;C snv 0.76 15
rs1032129
TNFRSF11B
0.851 0.040 8 118939661 intron variant A/C snv 0.37 5
rs5865
TMEM131
0.851 0.040 2 97756543 3 prime UTR variant C/T snv 0.62 5
rs865488
TG
0.882 8 132926377 intron variant C/T snv 0.67 4
rs1689510
SUOX
0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs7568275
STAT4
0.827 0.120 2 191101726 intron variant G/C;T snv 5
rs9507287
SPATA13
0.851 0.040 13 24212439 intron variant T/C snv 0.24 5
rs72743477
SMAD3
0.724 0.240 15 67171953 intron variant A/G snv 0.17 14
rs11746555
SLC22A5
0.882 5 132391341 intron variant G/A snv 0.28 4
rs7310615
SH2B3
0.882 12 111427245 intron variant C/G snv 0.67 12
rs6914622
SASH1
0.851 0.040 6 148193165 regulatory region variant G/T snv 0.33 5
rs11073337
RASGRP1
0.851 0.040 15 38555562 intron variant A/C snv 0.27 5
rs13380830
RAB5C
0.882 17 42145640 intron variant C/G snv 0.29 4
rs773107
RAB5B
0.882 12 55975722 intron variant A/G;T snv 4
rs67927699
PUS10
0.882 2 60960280 intron variant G/C;T snv 4
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs1443438
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv 5
rs13299616
PSMD5 ; CUTALP
0.882 9 120832525 intron variant T/C snv 0.50 4
rs4761587
PLXNC1
0.882 12 94158023 intron variant A/G snv 0.78 4