Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10414065 0.882 0.080 19 33230549 upstream gene variant C/T snv 5.5E-02 4
rs2918302
LINC01862 ; LOC107983991
0.925 0.080 19 8675909 intron variant G/A snv 0.19 2
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs892225
SBNO2
0.925 0.080 19 1152657 intron variant A/G snv 0.39 2
rs10411428 1.000 0.080 19 52104512 intergenic variant C/T snv 0.18 1
rs10413947 1.000 0.080 19 9017666 upstream gene variant G/A;T snv 1
rs11666341 1.000 0.080 19 52098146 upstream gene variant G/A snv 0.18 1
rs12460587
ZNF432 ; ZNF841
1.000 0.080 19 52083666 intron variant T/C;G snv 0.16 1
rs1800470
TGFB1
0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 1
rs2288884
ZNF614 ; LOC112268244
1.000 0.080 19 52029018 intron variant C/T snv 0.14 1
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 1
rs1893217
PTPN2
0.742 0.440 18 12809341 intron variant A/G snv 0.12 10
rs4574025
TNFRSF11A
0.882 0.160 18 62342581 intron variant C/T snv 0.55 4
rs12964116
SERPINB7
0.925 0.080 18 63775385 5 prime UTR variant A/G snv 3.0E-02 2
rs12965763
POLI
0.925 0.080 18 54290038 intron variant G/A snv 0.18 2
rs1893380 0.925 0.080 18 51121270 intergenic variant G/A;C;T snv 2
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 2
rs11877305 1.000 0.080 18 77739121 intergenic variant G/A snv 7.0E-02 1
rs2586731 1.000 0.080 18 50790789 downstream gene variant G/C;T snv 0.91 1
rs356150 1.000 0.080 18 77661491 intergenic variant C/A;G snv 1
rs4368243 1.000 0.080 18 40803519 intergenic variant T/A;C snv 1
rs643507
LPIN2 ; CHORDC1P4
1.000 0.080 18 2946293 non coding transcript exon variant C/T snv 0.96 0.92 1
rs7506840
LINC01387
1.000 0.080 18 6522757 intron variant G/A snv 0.11 1
rs9949526
LOC105372228
1.000 0.080 18 79614321 downstream gene variant C/A;T snv 1
rs9952762 1.000 0.080 18 75689695 intergenic variant C/A snv 5.9E-02 1