Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 24
rs28929474
SERPINA1
0.708 0.320 14 94378610 missense variant C/G;T snv 2.8E-05; 1.1E-02 17
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 13
rs34811474
ANAPC4
1.000 0.040 4 25407216 missense variant G/A;T snv 0.15; 4.1E-06 8
rs13108218
HGFAC
4 3442204 intron variant A/G;T snv 7
rs2145272 20 6645571 intergenic variant G/A;T snv 7
rs2294214
CASC15
0.882 0.040 6 22056694 splice region variant A/C;T snv 6
rs7740107
L3MBTL3
1.000 0.080 6 130053316 intron variant T/A;G snv 6
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 5
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs2812208
DLEU1
13 50132951 intron variant G/A;C snv 5
rs5742915
PML
0.925 0.080 15 74044292 missense variant T/C;G snv 0.35; 4.0E-06 5
rs72755233
ADAMTS17
1.000 0.080 15 100152748 missense variant G/A;T snv 7.1E-02; 3.2E-05 5
rs9292468 5 32818967 intergenic variant T/A;C snv 5
rs11152213 1.000 0.080 18 60185715 intergenic variant A/C;T snv 4
rs1126464
DPEP1
1.000 0.040 16 89637957 missense variant G/A;C snv 1.3E-05; 0.26 4
rs1351394
HMGA2
12 65958046 3 prime UTR variant T/C;G snv 4
rs7162542
ADAMTSL3
15 83845538 intron variant C/A;G;T snv 4
rs74929147 19 18302251 downstream gene variant G/A;C snv 4
rs10010325
TET2 ; TET2-AS1
1.000 0.040 4 105185196 intron variant C/A;G;T snv 3
rs10283100
ENPP2
8 119583783 missense variant A/G;T snv 0.96 3
rs10512248
PTCH1
0.925 0.120 9 95497421 intron variant T/A;G snv 3
rs10739217
LOC107987108
0.925 0.040 9 105973112 regulatory region variant T/A;C snv 3