Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7042370
LURAP1L-AS1 ; LURAP1L
0.724 0.240 9 12785074 intron variant T/C snv 0.58 14
rs117372389
NKD1
0.724 0.240 16 50634166 3 prime UTR variant G/T snv 1.1E-02 14
rs72743477
SMAD3
0.724 0.240 15 67171953 intron variant A/G snv 0.17 14
rs1250563
ZMIZ1
0.724 0.240 10 79287626 intron variant G/C snv 0.24 14
rs11065979 0.851 0.200 12 111621753 intergenic variant C/T snv 0.30 12
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs10748781 0.763 0.160 10 99523573 upstream gene variant C/A;G snv 11
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 11
rs174535
MYRF ; TMEM258
0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 11
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs4129267
IL6R
0.807 0.200 1 154453788 intron variant C/G;T snv 10
rs4845604
RORC
0.776 0.200 1 151829204 intron variant G/A;C;T snv 10
rs61839660
IL2RA
0.776 0.280 10 6052734 intron variant C/T snv 5.7E-02 9
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 9
rs11236797 0.790 0.200 11 76588605 upstream gene variant C/A snv 0.39 8
rs11221332
ETS1
0.763 0.280 11 128511079 intron variant C/A;T snv 8
rs11168249
HDAC7
0.807 0.120 12 47814585 intron variant T/C snv 0.50 8
rs17622378
IRF1-AS1
0.790 0.200 5 132442760 intron variant A/G snv 0.28 8
rs6651252
LINC00824
0.790 0.200 8 128554935 intron variant T/C snv 0.19 8
rs17293632
SMAD3
0.763 0.240 15 67150258 intron variant C/T snv 0.17 8
rs34920465 0.807 0.160 1 22373858 intergenic variant A/G snv 0.24 7
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 7
rs71624119
ANKRD55
0.776 0.200 5 56144903 intron variant G/A snv 0.17 7
rs1883832
CD40
0.581 0.680 20 46118343 5 prime UTR variant T/C snv 0.75 0.80 7
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 7