Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8170
BABAM1 ; USHBP1
0.724 0.160 19 17278895 synonymous variant G/A snv 0.15 0.18 3
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 1
rs7230264 1.000 0.120 18 27347470 intron variant G/A snv 0.15 1
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 4
rs183211
LRRC37A2 ; NSF
0.882 0.160 17 46710944 intron variant G/A snv 0.28 0.30 3
rs7405776
HNF1B
0.807 0.120 17 37733029 intron variant G/A;C snv 3
rs757210
HNF1B
0.807 0.160 17 37736525 intron variant C/G;T snv 2
rs9303542
SKAP1
0.882 0.120 17 48334138 intron variant A/G snv 0.34 2
rs8044477 1.000 0.120 16 58942687 intron variant A/G snv 0.53 1
rs11175194
SRGAP1
0.925 0.120 12 63871057 intron variant G/A snv 0.15 1
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 1
rs1834481
IL18
0.882 0.160 11 112153104 non coding transcript exon variant C/G snv 0.16 1
rs1243180
MLLT10
0.790 0.160 10 21626690 intron variant T/A snv 0.23 2
rs1192691 0.925 0.120 10 36880367 regulatory region variant G/T snv 0.90 1
rs4525119
LOC107984198 ; AKR1C3
0.925 0.120 10 5049762 intron variant C/T snv 0.30 1
rs9787692 1.000 0.120 10 8603200 intergenic variant T/G snv 0.30 1
rs3814113 0.827 0.200 9 16915023 upstream gene variant T/C snv 0.41 2
rs1413299
COL15A1
0.925 0.120 9 98998959 intron variant G/A;T snv 1
rs2070074
GALT
0.742 0.360 9 34649445 missense variant A/G snv 9.2E-02 7.4E-02 1
rs633862 0.925 0.120 9 133279871 upstream gene variant T/C snv 0.49 1
rs10088218
LINC00824
0.851 0.120 8 128531703 intron variant G/A snv 0.13 2
rs11782652
CHMP4C
0.851 0.120 8 81741409 intron variant A/G snv 6.6E-02 2
rs10260419
THSD7A
0.882 0.120 7 11524758 intron variant C/G snv 0.26 1
rs662
PON1
0.485 0.840 7 95308134 missense variant T/C snv 0.38 0.42 1