Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs855791
TMPRSS6
0.701 0.400 22 37066896 missense variant A/G;T snv 0.57; 4.0E-06 17
rs4148325
UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A1 ; UGT1A9 ; UGT1A3 ; UGT1A4 ; UGT1A6
0.851 0.080 2 233764663 intron variant C/T snv 0.36 8
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 8
rs4149056
SLCO1B1
0.633 0.480 12 21178615 missense variant T/C snv 0.13 0.12 7
rs929596
UGT1A5 ; UGT1A4 ; UGT1A9 ; UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A1
0.925 0.040 2 233765830 intron variant A/G snv 0.32 7
rs17863787
UGT1A9 ; UGT1A8 ; UGT1A6 ; UGT1A7 ; UGT1A10
0.925 0.040 2 233702448 intron variant T/G snv 0.30 7
rs2741012 1.000 2 233600317 upstream gene variant C/T snv 0.24 5
rs4663969
UGT1A6 ; UGT1A9 ; UGT1A3 ; UGT1A10 ; UGT1A5 ; UGT1A4 ; UGT1A8 ; UGT1A7
1.000 2 233746667 intron variant C/A;T snv 5
rs3755319
UGT1A8 ; UGT1A1 ; UGT1A3 ; UGT1A4 ; UGT1A7 ; UGT1A10 ; UGT1A9 ; UGT1A5 ; UGT1A6
0.925 0.120 2 233758936 intron variant A/C;G;T snv 5
rs4477910
UGT1A9 ; UGT1A10 ; UGT1A7 ; UGT1A4 ; UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A3
1.000 2 233735091 intron variant A/T snv 0.46 5
rs1875263
UGT1A9 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A6 ; UGT1A8 ; UGT1A4
1.000 2 233716976 intron variant C/G;T snv 5
rs10173355
UGT1A9 ; UGT1A7 ; UGT1A10 ; UGT1A8
1.000 2 233688675 intron variant A/G;T snv 5
rs13394720 1.000 2 233593475 intergenic variant T/C snv 7.0E-02 4
rs2070959
UGT1A8 ; UGT1A7 ; UGT1A9 ; UGT1A10 ; UGT1A6
0.742 0.320 2 233693545 missense variant A/G snv 0.31 0.30 3
rs13189262 1.000 0.040 5 57978493 intergenic variant G/T snv 0.16 2
rs16885704 1.000 0.040 6 74829426 regulatory region variant A/G snv 6.1E-02 2
rs2741027 1.000 0.040 2 233609365 downstream gene variant G/A snv 0.22 2
rs2963791 1.000 0.040 5 3844427 regulatory region variant C/A snv 0.80 2
rs2978048 1.000 0.080 8 133603893 intergenic variant T/C;G snv 5.2E-02 2
rs359935 1.000 0.040 1 89517625 intron variant G/A;T snv 2
rs6585514 1.000 0.040 10 118836874 intron variant A/G snv 0.62 2
rs7262634 1.000 0.080 20 47205635 downstream gene variant T/C snv 8.6E-02 2
rs9957684 1.000 0.040 18 75154908 intergenic variant C/T snv 6.9E-02 2
rs9903658
ASIC2
1.000 0.040 17 33729207 intron variant A/G snv 0.11 2
rs658995
CBLN2
1.000 0.040 18 72540105 non coding transcript exon variant A/G;T snv 2