Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs6434742
LOC105376755
1.000 0.080 2 195172179 intergenic variant A/G snv 0.93 1
rs2780293 1.000 0.080 1 56439400 intron variant A/G snv 0.92 1
rs1423096 0.925 0.080 19 7674291 upstream gene variant T/C snv 0.92 1
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 6
rs7921488
CUBN
1.000 0.080 10 17127078 intron variant A/G snv 0.90 1
rs10761745
JMJD1C
0.882 0.240 10 63341311 intron variant G/C snv 0.87 1
rs2867125 0.925 0.120 2 622827 intergenic variant T/A;C snv 0.85 3
rs2820001
CDKAL1 ; LOC107986577
1.000 0.080 6 20758712 intron variant G/T snv 0.85 1
rs234146
LOC105370650 ; LINC02291
1.000 0.080 14 97688175 intron variant T/C snv 0.85 1
rs2925757 1.000 0.080 2 160244658 intron variant G/A snv 0.84 1
rs1727313
MPHOSPH9
1.000 0.080 12 123156306 3 prime UTR variant C/G snv 0.84 1
rs10767664
BDNF
0.752 0.400 11 27704439 intron variant T/A snv 0.83 2
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 12
rs7025162 1.000 0.080 9 133290774 regulatory region variant T/C snv 0.82 3
rs10190052 1.000 0.080 2 646674 intergenic variant T/C snv 0.82 1
rs7561317 0.925 0.120 2 644953 intergenic variant A/G snv 0.81 4
rs495828 0.827 0.200 9 133279294 upstream gene variant T/G snv 0.81 8
rs831571 1.000 0.080 3 64062621 intergenic variant T/C snv 0.81 1
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs4688985
WFS1
1.000 0.080 4 6283988 intron variant A/G snv 0.79 1
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 8
rs10181656
STAT4
0.763 0.360 2 191105153 intron variant G/C snv 0.79 1
rs3130501
POU5F1
0.851 0.280 6 31168676 intron variant A/G snv 0.78 3