Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 7
rs113296370
PLEKHH2
1.000 0.040 2 43636315 upstream gene variant A/C snv 0.17 3
rs4833103
TLR1
0.925 0.160 4 38813881 intron variant A/C snv 0.64 3
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 1
rs2542713
DAB2 ; C9
1.000 0.040 5 39385539 intron variant A/C;G snv 3
rs497309
CYP21A2 ; C2
0.882 0.240 6 31924707 intron variant A/C;G snv 3
rs6688849 1.000 0.040 1 47530532 intergenic variant A/C;G snv 2
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 1
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 8
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 7
rs10811652
CDKN2B-AS1
0.882 0.120 9 22077086 intron variant A/C;T snv 3
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 3
rs2237895
KCNQ1
0.790 0.240 11 2835964 intron variant A/C;T snv 1
rs6476839
GLIS3
0.925 0.120 9 4290823 intron variant A/C;T snv 1
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 30
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 19
rs261332
ALDH1A2 ; LIPC-AS1 ; LIPC
0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 17
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 17
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 16
rs2111485 0.724 0.280 2 162254026 regulatory region variant A/G snv 0.46 12
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10