Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1569414
FAM118A
0.807 0.160 22 45331684 intron variant T/G snv 0.44 6
rs2072693
RHCG
1.000 0.040 15 89471714 3 prime UTR variant T/G snv 0.60 1
rs9831002 1.000 0.040 3 18811205 intron variant T/G snv 0.59 1
rs62106258 1.000 0.040 2 417167 upstream gene variant T/C snv 2.9E-02 5
rs1108343 1.000 0.040 16 51177684 non coding transcript exon variant T/C snv 0.52 1
rs1126478
LTF
0.763 0.240 3 46459723 missense variant T/C snv 0.41 0.51 1
rs1884302 0.851 0.120 20 7125642 intron variant T/C snv 0.41 1
rs34559440 1.000 0.040 17 70402971 intergenic variant T/C snv 0.28 1
rs3820640
ITPKB
1.000 0.040 1 226681217 intron variant T/C snv 0.12 1
rs4251631
CDKN3
1.000 0.040 14 54409466 intron variant T/C snv 0.28 1
rs57067187
LOC100130370
1.000 0.040 17 81387532 non coding transcript exon variant T/C snv 0.28 1
rs72748935
CA12
1.000 0.040 15 63347217 intron variant T/C snv 0.39 1
rs7918807 1.000 0.040 10 9978231 intergenic variant T/C snv 0.53 1
rs1429138 1.000 0.040 4 147361190 regulatory region variant T/A;C snv 1
rs121908120
WNT10A
0.701 0.280 2 218890289 missense variant T/A snv 1.4E-02 1.4E-02 11
rs10772314
LOC105369658 ; LINC02446
1.000 0.040 12 10551751 upstream gene variant T/A snv 0.47 1
rs10987008
PBX3
1.000 0.040 9 125899321 intron variant T/A snv 0.54 1
rs140357883
MTMR3
1.000 0.040 22 29896823 intron variant T/-;TT;TTT delins 1
rs399593
LYZL2
1.000 0.040 10 30623101 intron variant G/T snv 0.86 1
rs9366651
LOC107986582
1.000 0.040 6 26336468 upstream gene variant G/T snv 0.49 1
rs1482698
LINC02224
1.000 0.040 5 44539351 intron variant G/C snv 0.30 1
rs8054556
TMEM219
0.925 0.080 16 29946895 intron variant G/A;C;T snv 4
rs185566659
OPA1 ; LOC102724808
1.000 0.040 3 193676936 intron variant G/A;C snv 1
rs10851907
CHRNB4
1.000 0.040 15 78623522 upstream gene variant G/A snv 0.40 4
rs149467613
P2RY2
1.000 0.040 11 73232438 intron variant G/A snv 3.3E-02 2