Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2235529
WNT4
1.000 0.040 1 22123994 intron variant C/T snv 0.13 1
rs2894204
HLA-C
1.000 0.040 6 31269284 intron variant C/A;T snv 1
rs3786897
PEPD
1.000 0.080 19 33402102 intron variant A/G snv 0.45 1
rs605203
EHMT2-AS1 ; LOC107986588 ; CYP21A2 ; SLC44A4
1.000 0.120 6 31879235 intron variant C/A snv 0.77 1
rs6784615
NISCH
1.000 0.080 3 52472410 intron variant C/T snv 0.96 0.96 1
rs7637773
IGF2BP2
1.000 0.080 3 185797847 intron variant G/A snv 0.38 1
rs9302652
FTO
1.000 0.080 16 53832063 intron variant C/T snv 0.74 1
rs9750952 1.000 0.080 2 238827723 intergenic variant C/T snv 0.19 1
rs1051921
MLXIPL
0.925 0.120 7 73593613 3 prime UTR variant G/A snv 0.15 6
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5
rs10195252
COBLL1
0.925 0.080 2 164656581 intron variant T/C snv 0.48 3
rs2112347
POC5 ; LOC441087
0.925 0.120 5 75719417 upstream gene variant T/G snv 0.42 3
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 3
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 1
rs459193
C5orf67
0.925 0.120 5 56510924 downstream gene variant A/G snv 0.69 1
rs620861
PCAT1 ; CASC8 ; POU5F1B ; CASC21
0.925 0.080 8 127323428 intron variant G/A snv 0.36 1
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs9515201
COL4A2
0.925 0.080 13 110388451 intron variant A/C snv 0.63 1
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 3
rs17249754
ATP2B1
0.882 0.120 12 89666809 intron variant G/A snv 0.15 3
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 3
rs727428 0.882 0.200 17 7634474 downstream gene variant T/C snv 0.55 3
rs9369425
LOC107986598
0.882 0.160 6 43843237 downstream gene variant G/A snv 0.66 3
rs6905288 0.882 0.120 6 43791136 downstream gene variant G/A snv 0.56 2
rs718314
LOC105369705
0.882 0.120 12 26300350 intron variant A/G snv 0.27 2