Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13417564
LOC105374780
2 65438139 intron variant G/T snv 0.57 2
rs35389394
CCDC26
8 129609008 intron variant C/T snv 0.56 2
rs6584283
LINC01475
0.776 0.080 10 99530544 intron variant T/C snv 0.56 12
rs34301845
MIR3936HG ; SLC22A4
5 132329474 intron variant TT/-;T;TTT;TTTT;TTTTTTTTTTTTTT delins 0.56 2
rs4703904
ZNF366
5 72466717 intron variant G/A snv 0.56 2
rs1375493
ITGA4
2 181459039 non coding transcript exon variant G/A snv 0.56 3
rs1449263 1.000 0.080 2 181454574 upstream gene variant C/T snv 0.56 3
rs10562650
ITGA4
2 181459460 intron variant TT/-;T;TTT delins 0.56 2
rs3095254 6 31253891 intergenic variant C/A;G snv 0.55 2
rs2124440
ITGA4
2 181463487 intron variant G/A snv 0.55 2
rs12916091 15 79930230 downstream gene variant T/G snv 0.53 2
rs1037171
CD300LF ; RAB37
17 74706839 intron variant G/A snv 0.53 2
rs424971
IRF8
16 85912844 intron variant T/C snv 0.53 2
rs2038700
STXBP6
14 24992783 intron variant T/C snv 0.53 7
rs13277237
CCDC26
8 129592317 intron variant G/A snv 0.53 4
rs7516138
PIK3CD
1 9651584 upstream gene variant A/G snv 0.52 2
rs7919533
CDH23 ; VSIR
10 71765768 intron variant T/C snv 0.52 2
rs2004925
STXBP6
14 24976156 intron variant G/A snv 0.52 2
rs4432538
PLCB1 ; LOC105372521
20 8626746 intron variant G/A snv 0.52 4
rs913678 0.882 0.240 20 50338887 regulatory region variant T/C snv 0.51 5
rs2632516
TSPOAP1-AS1 ; MIR142
1.000 0.080 17 58331728 non coding transcript exon variant G/A;C snv 0.51 3
rs4812447
LOC102724968
20 40643980 regulatory region variant A/G snv 0.51 2
rs8064299
SLC9A3R1
17 74766507 intron variant C/A snv 0.50 2
rs5769707
C22orf34
22 49619754 non coding transcript exon variant G/T snv 0.50 2
rs10751647
IFITM2
11 306884 upstream gene variant T/C snv 0.49 2