Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs200426271
MTMR3
1.000 0.080 22 29948468 intron variant -/G ins 1
rs8321
ZNRD1
0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 11
rs2523987
TRIM31-AS1 ; TRIM31
0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 5
rs6495314
CHRNB4 ; LOC112268142
0.925 0.080 15 78668187 intron variant A/C snv 0.35 3
rs1105879
UGT1A9 ; UGT1A6 ; UGT1A7 ; UGT1A10 ; UGT1A8
0.790 0.240 2 233693556 missense variant A/C snv 0.35 0.34 2
rs17486278
CHRNA5
0.827 0.120 15 78575140 intron variant A/C snv 0.32 2
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 1
rs213210
MIR219A1 ; RING1
0.742 0.240 6 33208047 upstream gene variant A/C;G snv 1
rs2844573 0.882 0.160 6 31367677 intron variant A/C;G snv 1
rs718772
HORMAD2
0.925 0.120 22 30108218 intron variant A/C;G snv 1
rs8138286
HORMAD2
1.000 0.080 22 30166998 intron variant A/C;G snv 0.20 1
rs28366298
HLA-DRB1
0.925 0.120 6 32593082 upstream gene variant A/C;T snv 3
rs4887053 0.925 0.080 15 78420357 regulatory region variant A/C;T snv 3
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 2
rs12901682
PSMA4
0.851 0.200 15 78540881 5 prime UTR variant A/C;T snv 1
rs8042059
CHRNA3
0.882 0.080 15 78615517 intron variant A/C;T snv 1
rs389884
STK19 ; CYP21A2 ; DXO
0.776 0.440 6 31973120 non coding transcript exon variant A/G snv 7.1E-02 7
rs1235162
GABBR1
0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 6
rs1270942
CFB ; CYP21A2
0.742 0.440 6 31951083 non coding transcript exon variant A/G snv 7.5E-02 6
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 5
rs3132610
ABCF1
0.807 0.280 6 30576624 intron variant A/G snv 7.4E-02 5
rs8042374
CHRNA3
0.807 0.200 15 78615690 intron variant A/G snv 0.29 4
rs10484399 0.851 0.240 6 27566749 intergenic variant A/G snv 5.4E-02 3
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 3
rs1233579 0.925 0.160 6 28744886 intergenic variant A/G snv 7.2E-02 3