Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121908120
WNT10A
0.701 0.280 2 218890289 missense variant T/A snv 1.4E-02 1.4E-02 11
rs1569414
FAM118A
0.807 0.160 22 45331684 intron variant T/G snv 0.44 6
rs62106258 1.000 0.040 2 417167 upstream gene variant T/C snv 2.9E-02 5
rs10851907
CHRNB4
1.000 0.040 15 78623522 upstream gene variant G/A snv 0.40 4
rs8054556
TMEM219
0.925 0.080 16 29946895 intron variant G/A;C;T snv 4
rs11676272
ADCY3
1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 3
rs10048146 1.000 0.040 16 86677054 regulatory region variant A/G snv 0.17 2
rs3114018
ABCG2
0.882 0.160 4 88143429 intron variant A/C snv 0.48 2
rs149467613
P2RY2
1.000 0.040 11 73232438 intron variant G/A snv 3.3E-02 2
rs931608
ZNF98
1.000 0.040 19 22431320 intron variant A/C;T snv 2
rs10180496 1.000 0.040 2 12828774 intron variant A/G snv 0.15 1
rs10811723 1.000 0.040 9 22542286 intergenic variant A/G snv 0.55 1
rs1108343 1.000 0.040 16 51177684 non coding transcript exon variant T/C snv 0.52 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
rs1352724 1.000 0.040 5 107747786 intergenic variant C/A snv 0.15 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
rs263771 1.000 0.040 2 185056965 intergenic variant C/A;T snv 1
rs28822480 1.000 0.040 18 60257590 intergenic variant G/A snv 0.25 1
rs34559440 1.000 0.040 17 70402971 intergenic variant T/C snv 0.28 1
rs4816017 1.000 0.040 20 7673726 intergenic variant G/A snv 0.24 1
rs5922945 1.000 0.040 X 84268007 intergenic variant C/T snv 0.25 1
rs72694438 1.000 0.040 1 103822256 intergenic variant G/A snv 0.18 1
rs7918807 1.000 0.040 10 9978231 intergenic variant T/C snv 0.53 1