Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10763957 10 33877770 regulatory region variant C/T snv 0.35 1
rs10788569
CFL1P1
10 87844975 non coding transcript exon variant T/C snv 0.23 2
rs10795055
LOC105376360
10 3539029 intron variant A/G snv 0.54 1
rs10804591 3 129615390 intergenic variant C/A snv 0.63 4
rs10808546 8 125483576 intron variant C/T snv 0.39 6
rs10820747
ABCA1
9 104924542 intron variant G/A snv 0.27 1
rs10827226
NRP1
10 33270391 intron variant T/A;C snv 1
rs10827252 10 33383956 upstream gene variant A/G snv 0.51 1
rs10828247
MLLT10
10 21533927 intron variant A/G snv 0.36 1
rs10840349
SBF2
11 10054883 intron variant A/G;T snv 1
rs10842707 12 26318431 intron variant C/G;T snv 4
rs10843817
CAPRIN2
12 30712576 intron variant A/C snv 0.21 1
rs10844642 12 33577433 downstream gene variant A/C snv 0.27 1
rs10850127
DTX1
12 113075140 intron variant C/T snv 0.20 1
rs10851523 15 52751805 downstream gene variant G/A;C snv 1
rs10863961
PPP2R5A
1 212294505 intron variant G/A snv 0.24 1
rs10872224 6 97987249 intron variant G/T snv 0.67 2
rs10875120
LINC01930 ; DPYD ; MIR137HG
1 97934347 intron variant G/T snv 0.72 1
rs10876528
HOXC6 ; HOXC5 ; HOXC4
12 54027692 intron variant C/A;G snv 2
rs10880321 12 37976308 intergenic variant C/A;G snv 1
rs10887759
CFL1P1
10 87843667 intron variant G/A snv 0.12 1
rs10891290
PPP2R1B
11 111734491 intron variant T/C snv 0.35 1
rs10891483
NCAM1
11 112967156 intron variant C/G;T snv 1
rs10894604
OPCML
11 132771851 non coding transcript exon variant T/G snv 0.26 1
rs10896012 11 65510990 downstream gene variant T/C snv 0.16 2