Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11755527
BACH2
0.851 0.360 6 90248512 intron variant C/G snv 0.36 3
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 3
rs12708716
CLEC16A
0.807 0.320 16 11086016 intron variant A/G snv 0.37 4
rs4712523
CDKAL1
0.925 0.120 6 20657333 intron variant A/G snv 0.41 3
rs3788013
UBASH3A
0.851 0.240 21 42421219 intron variant C/A snv 0.44 1
rs1990760
IFIH1
0.672 0.480 2 162267541 missense variant C/T snv 0.50 0.45 4
rs11894266 1.000 0.080 2 169780132 downstream gene variant C/T snv 0.45 2
rs3760627
CLPTM1
1.000 0.080 19 44953923 non coding transcript exon variant T/C snv 0.80 0.51 2
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 3
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 1
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 6
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs689
INS ; INS-IGF2
0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60 1
rs4689388
WFS1
0.882 0.360 4 6268329 upstream gene variant G/A snv 0.64 3
rs2582367 1.000 0.080 8 27622508 regulatory region variant C/T snv 0.64 2
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 4
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 3
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 4
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 3
rs543293 0.925 0.080 11 86109035 regulatory region variant A/G snv 0.72 2
rs7941541 11 86147496 intergenic variant G/A snv 0.73 1
rs2542151 0.763 0.480 18 12779948 upstream gene variant G/T snv 0.83 6
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13