Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17885785
IGF2 ; IGF2-AS ; INS-IGF2
0.724 0.240 11 2146620 non coding transcript exon variant C/T snv 0.14 14
rs72920202
JAK1
0.882 1 64895266 intron variant A/T snv 0.15 4
rs71508903
ARID5B
0.807 0.160 10 62020112 intron variant C/T snv 0.15 7
rs55984493 0.851 0.040 13 99118074 intergenic variant A/T snv 0.15 5
rs6840978
IL21-AS1
0.776 0.160 4 122633552 intron variant C/T snv 0.16 4
rs12863738 0.724 0.240 X 136949968 intron variant C/T snv 0.16 14
rs28583049
LOC105374033
0.882 3 108724568 downstream gene variant T/C snv 0.17 4
rs77150043
ADCY7
0.724 0.240 16 50270338 intron variant C/T snv 0.17 14
rs72743477
SMAD3
0.724 0.240 15 67171953 intron variant A/G snv 0.17 14
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
rs7672495 0.724 0.240 4 4990640 regulatory region variant T/C snv 0.21 14
rs7655915
LOC107986195
0.882 4 148712316 intron variant C/T snv 0.22 4
rs2836882 0.724 0.240 21 39094644 intergenic variant G/A snv 0.23 15
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs9507287
SPATA13
0.851 0.040 13 24212439 intron variant T/C snv 0.24 5
rs1689510
SUOX
0.724 0.240 12 56002984 non coding transcript exon variant G/C snv 0.25 16
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs4676410
GPR35
0.716 0.240 2 240624322 intron variant G/A snv 0.26 17
rs11073337
RASGRP1
0.851 0.040 15 38555562 intron variant A/C snv 0.27 5
rs10986284 0.882 9 124236874 intergenic variant A/T snv 0.27 4
rs11746555
SLC22A5
0.882 5 132391341 intron variant G/A snv 0.28 4
rs755374 0.724 0.240 5 159402286 intron variant C/T snv 0.28 14
rs11741255
IRF1-AS1
0.724 0.240 5 132475490 intron variant G/A snv 0.29 14
rs13380830
RAB5C
0.882 17 42145640 intron variant C/G snv 0.29 4