Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10822050 0.724 0.240 10 62679011 downstream gene variant T/C snv 0.33 14
rs1332099 0.724 0.240 10 99538694 downstream gene variant T/C;G snv 14
rs2738774 0.724 0.240 20 63637985 downstream gene variant G/A;C snv 14
rs2807264 0.724 0.240 X 136583619 downstream gene variant C/A snv 14
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 7
rs113010081 0.925 0.160 3 46415921 downstream gene variant T/C snv 7.3E-02 3
rs2856718 0.790 0.360 6 32702478 downstream gene variant C/T snv 0.34 2
rs917997 0.701 0.480 2 102454108 downstream gene variant T/A;C snv 2
rs11954020 1.000 0.120 5 35883149 downstream gene variant C/G;T snv 1
rs2248462 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 1
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 1
rs7090530 0.851 0.160 10 6068912 downstream gene variant C/A snv 0.59 1
rs72853903 1.000 0.120 11 2177435 downstream gene variant C/T snv 0.22 1
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 25
rs36051895 0.716 0.240 9 4981866 upstream gene variant G/T snv 0.25 15
rs7660520 0.724 0.240 4 182824168 upstream gene variant G/A;C snv 14
rs4728142 0.732 0.320 7 128933913 upstream gene variant G/A snv 0.38 11
rs3761980
MAPK14 ; SLC26A8
0.807 0.240 6 36026129 upstream gene variant A/G snv 0.14 7
rs694739
LOC102723878
0.763 0.320 11 64329761 upstream gene variant A/G snv 0.28 6
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 5
rs2736340 0.683 0.480 8 11486464 upstream gene variant C/T snv 0.25 4
rs10741657
CYP2R1
0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 3
rs3842727
TH
1.000 0.120 11 2163618 upstream gene variant G/T snv 0.58 3
rs3957148 0.925 0.160 6 32714360 upstream gene variant A/C;G snv 0.10 3
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 3