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
rs6495122 1.000 0.040 15 74833304 downstream gene variant A/C snv 0.44 3
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 2
rs9351814 0.882 0.040 6 71484004 intergenic variant A/C snv 0.35 2
rs10946398
CDKAL1
0.827 0.160 6 20660803 intron variant A/C snv 0.40 1
rs11591710 0.882 0.160 10 103927874 intergenic variant A/C snv 0.16 1
rs1648707 0.925 0.080 3 186833922 intergenic variant A/C snv 0.43 1
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 5
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 3
rs2246942
LIPA
0.925 0.040 10 89245129 intron variant A/C;G snv 1
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 3
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
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 3
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
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 12
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 10
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 10