Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2582367 1.000 0.080 8 27622508 regulatory region variant C/T snv 0.64 2
rs157580
TOMM40
0.882 0.160 19 44892009 intron variant G/A snv 0.69 11
rs3024505 0.790 0.320 1 206766559 upstream gene variant G/A snv 0.11 6
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs2927438 0.925 0.080 19 44738850 intergenic variant G/A snv 0.20 5
rs1004446
IGF2 ; INS-IGF2 ; IGF2-AS
0.827 0.240 11 2148913 intron variant G/A snv 0.37 3
rs4689388
WFS1
0.882 0.360 4 6268329 upstream gene variant G/A snv 0.64 3
rs12610605
NECTIN2
1.000 0.080 19 44867581 intron variant G/A snv 0.15 2
rs377702
NECTIN2
1.000 0.080 19 44859410 intron variant G/A snv 0.34 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
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 4
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 24
rs5167
APOC2 ; APOC4-APOC2 ; APOC4
1.000 0.040 19 44945208 missense variant T/A;G snv 3.6E-05; 0.39 3
rs2965101 1.000 0.080 19 44734556 intergenic variant T/C snv 0.34 6
rs439401 0.851 0.200 19 44911194 non coding transcript exon variant T/C snv 0.68 4
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 3
rs2943641 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 3
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 3
rs3760627
CLPTM1
1.000 0.080 19 44953923 non coding transcript exon variant T/C snv 0.80 0.51 2
rs12722495
IL2RA
0.851 0.200 10 6055320 intron variant T/C snv 7.0E-02 1
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 8
rs10402271 1.000 0.080 19 44825957 downstream gene variant T/G snv 0.28 6
rs1701704
LOC105369781 ; IKZF4
0.851 0.200 12 56018703 intron variant T/G snv 0.25 5
rs2292239
ERBB3
0.742 0.480 12 56088396 intron variant T/G snv 0.65 4