Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3114018
ABCG2
0.882 0.160 4 88143429 intron variant A/C snv 0.48 4
rs10048146 1.000 0.040 16 86677054 regulatory region variant A/G snv 0.17 2
rs11676272
ADCY3
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 2
rs10180496 1.000 0.040 2 12828774 intron variant A/G snv 0.15 1
rs11166135 1.000 0.040 1 98883280 intergenic variant A/G snv 0.10 1
rs12602978 1.000 0.040 17 27240054 intron variant C/T snv 9.3E-02 1
rs1429138 1.000 0.040 4 147361190 regulatory region variant T/A;C snv 1
rs1884302 0.851 0.120 20 7125642 intron variant T/C snv 0.41 1
rs9308447 1.000 0.040 1 9372331 downstream gene variant C/T snv 0.27 1
rs1383934
ADAMTS3
1.000 0.040 4 72551807 intron variant G/A snv 0.68 1
rs10242311
ATXN7L1
1.000 0.040 7 105633273 intron variant A/C snv 6.2E-02 1
rs4251631
CDKN3
1.000 0.040 14 54409466 intron variant T/C snv 0.28 1
rs17057381
EPHX2
1.000 0.040 8 27559284 upstream gene variant G/A snv 4.8E-02 1
rs9793739
LINC02815 ; LINC02814
1.000 0.040 1 229150111 intron variant G/A snv 9.6E-02 1
rs3896439
LOC107985376
1.000 0.040 1 4608610 intergenic variant G/A snv 9.4E-02 1
rs399593
LYZL2
1.000 0.040 10 30623101 intron variant G/T snv 0.86 1
rs713598
MGAM ; TAS2R38
0.851 0.160 7 141973545 missense variant C/G snv 0.46 0.44 1
rs980562
MPPED2
1.000 0.040 11 30435270 intron variant G/A snv 0.22 1
rs2735733
MUC5B
1.000 0.040 11 1240410 intron variant C/T snv 0.49 0.43 1
rs2857476
MUC5B
1.000 0.040 11 1259904 intron variant T/C snv 0.54 1
rs2531154
PROM1
1.000 0.040 4 16016701 intron variant C/T snv 0.89 1
rs635808
RPS6KA2
1.000 0.040 6 166763934 intron variant G/A snv 0.27 1
rs931608
ZNF98
1.000 0.040 19 22431320 intron variant A/C;T snv 1