Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1102705 0.925 0.080 1 172731728 intergenic variant G/A snv 0.93 3
rs2766678
ZNF217
20 53591817 intron variant G/A snv 0.86 1
rs2107357 16 27399508 upstream gene variant A/G snv 0.85 1
rs13403656
SOCAR ; MIR4435-2HG
2 111511550 intron variant A/T snv 0.84 1
rs2589561 1.000 0.080 10 9004682 intergenic variant A/G snv 0.83 1
rs5758343 22 41420648 intergenic variant A/T snv 0.82 1
rs697852
ITPKB
1 226727033 intron variant G/A snv 0.82 3
rs413382 1.000 0.080 9 6142948 intergenic variant C/A snv 0.81 1
rs20541
IL13 ; TH2LCRR
0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 4
rs9739070 12 123286485 upstream gene variant A/G snv 0.75 1
rs4848612
ANAPC1
2 111630961 non coding transcript exon variant G/A snv 0.74 1
rs1837253 0.790 0.240 5 111066174 upstream gene variant T/C snv 0.72 8
rs6489785 1.000 0.040 12 120925921 TF binding site variant T/C snv 0.68 3
rs6990534
PVT1
8 127801845 intron variant A/G snv 0.68 1
rs740474
DIAPH1
5 141545795 intron variant C/T snv 0.68 1
rs4236540
KPNA7
7 99171402 downstream gene variant G/T snv 0.68 1
rs11464691 17 40614389 intergenic variant -/A delins 0.68 1
rs848
IL13 ; TH2LCRR
0.807 0.240 5 132660808 3 prime UTR variant A/C snv 0.67 2
rs1147169
PLCL1
2 198036671 intron variant T/C snv 0.67 1
rs9911533 1.000 0.080 17 40619224 intergenic variant C/T snv 0.67 2
rs10068717
NDFIP1
5 142115369 intron variant C/T snv 0.67 1
rs13384448 2 227843146 intergenic variant C/T snv 0.67 1
rs12440045 0.925 0.080 15 41490486 upstream gene variant A/C snv 0.67 6
rs10008032
LOC105374413
1.000 0.080 4 38743861 intergenic variant T/C snv 0.66 2
rs2197415 10 9020893 intergenic variant T/G snv 0.66 1