Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs11591710 0.882 0.160 10 103927874 intergenic variant A/C snv 0.16 1
rs190996050 1.000 0.040 5 1048492 downstream gene variant T/C snv 5.7E-03 1
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 23
rs78442819
TEKT5
1.000 0.040 16 10647125 intron variant G/C snv 0.13 2
rs3827760
RANBP2 ; EDAR
0.752 0.160 2 108897145 missense variant A/G snv 0.15 5.9E-02 6
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 3
rs9387478
DCBLD1
0.851 0.080 6 117465017 intron variant C/A;T snv 2
rs9387479
DCBLD1
1.000 0.040 6 117471449 intron variant T/C;G snv 1
rs55768116
MPZL3
0.925 0.080 11 118237616 intron variant C/A snv 0.38 2
rs1056562
MPZL2
1.000 0.040 11 118254910 3 prime UTR variant T/C snv 0.57 1
rs114928225 1.000 0.040 2 118692164 intergenic variant T/A snv 1.0E-02 1
rs11200014
FGFR2
0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 17
rs2608029
PVT1
1.000 0.040 8 128157880 intron variant C/G snv 0.37 2
rs7725218
TERT
0.708 0.280 5 1282299 intron variant G/A snv 0.38 17
rs67824503
LINC00824
1.000 0.040 8 128523018 intron variant T/C snv 0.23 1
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 12
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 6
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 4
rs16906252
MGMT
0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 2
rs4635969 0.827 0.160 5 1308437 downstream gene variant G/A;T snv 2
rs4975616 0.763 0.320 5 1315545 downstream gene variant G/A snv 0.51 1