Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8106922
TOMM40
1.000 0.080 19 44898409 intron variant A/G snv 0.36 4
rs8103315
BCL3
1.000 0.080 19 44750911 intron variant C/A snv 9.1E-02 2
rs7941541 11 86147496 intergenic variant G/A snv 0.73 1
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 8
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs7528684
FCRL3
0.752 0.560 1 157701026 upstream gene variant A/G snv 0.57 1
rs7171171
LOC107984725
0.925 0.120 15 38614840 intergenic variant A/G snv 0.24 1
rs689
INS ; INS-IGF2
0.776 0.280 11 2160994 splice region variant A/T snv 0.73 0.60 1
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 6
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 14
rs543293 0.925 0.080 11 86109035 regulatory region variant A/G snv 0.72 2
rs5167
APOC2 ; APOC4-APOC2 ; APOC4
1.000 0.040 19 44945208 missense variant T/A;G snv 3.6E-05; 0.39 3
rs4788084
IL27
0.827 0.200 16 28528527 downstream gene variant C/T snv 0.36 3
rs4712523
CDKAL1
0.925 0.120 6 20657333 intron variant A/G snv 0.41 3
rs4689388
WFS1
0.882 0.360 4 6268329 upstream gene variant G/A snv 0.64 3
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 4
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 3
rs3788013
UBASH3A
0.851 0.240 21 42421219 intron variant C/A snv 0.44 1
rs377702
NECTIN2
1.000 0.080 19 44859410 intron variant G/A snv 0.34 2
rs3760627
CLPTM1
1.000 0.080 19 44953923 non coding transcript exon variant T/C snv 0.80 0.51 2
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6