Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3923113 0.882 0.120 2 164645339 intergenic variant A/C;G;T snv 1
rs4478891
CDC123
1.000 0.080 10 12225655 intron variant A/C;G;T snv 1
rs6673820
SLC26A9 ; SLC26A9-AS1
1.000 0.080 1 205941476 intron variant A/C;G;T snv 1
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 6
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 5
rs10738610
CDKN2B-AS1
0.882 0.120 9 22123767 intron variant A/C;T snv 3
rs7741604
CDKAL1
0.925 0.120 6 20731293 intron variant A/C;T snv 2
rs10908278
HNF1B
0.925 0.160 17 37739961 intron variant A/C;T snv 1
rs1874361
SLC26A9 ; SLC26A9-AS1
1.000 0.080 1 205939058 intron variant A/C;T snv 1
rs2237895
KCNQ1
0.790 0.240 11 2835964 intron variant A/C;T snv 1
rs6767577
IGF2BP2
1.000 0.080 3 185802944 intron variant A/C;T snv 1
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 15
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 8
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 7
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 6
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 6
rs2260000
PRRC2A
0.851 0.200 6 31625699 intron variant A/G snv 0.29 6
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 5
rs11075990
FTO
0.925 0.120 16 53785981 intron variant A/G snv 0.41 5
rs11558471
LOC105375716 ; SLC30A8
1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 5
rs4430796
HNF1B
0.790 0.280 17 37738049 intron variant A/G snv 0.52 5
rs7202116
FTO
0.882 0.120 16 53787703 intron variant A/G snv 0.41 5
rs780092
GCKR
0.827 0.160 2 27520287 intron variant A/G snv 0.18 5