Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2847281
PTPN2
1.000 0.040 18 12821594 intron variant A/G snv 0.32 2
rs12210050
LOC105374875
0.807 0.040 6 475489 non coding transcript exon variant C/T snv 0.11 1
rs17761864
SMG6
1.000 0.040 17 2268343 intron variant C/A snv 0.28 1
rs2239612
ST6GAL1
1.000 0.040 3 187075454 intron variant G/A snv 0.17 1
rs4785204
HEATR3
1.000 0.040 16 50069823 intron variant C/T snv 8.6E-02 1
rs6503659 1.000 0.040 17 41741012 intergenic variant A/C;G;T snv 1
rs7335046 0.807 0.040 13 99389484 downstream gene variant G/C snv 0.80 1
rs1042602
LOC107984363 ; TYR
0.925 0.080 11 89178528 missense variant C/A snv 0.25 0.24 2
rs1050631
SLC39A6
0.882 0.080 18 36114157 synonymous variant G/A snv 0.33 0.30 1
rs12296850 0.925 0.080 12 100426307 downstream gene variant A/G snv 8.7E-02 1
rs2239815
XBP1
0.925 0.080 22 28796682 non coding transcript exon variant T/C snv 0.44 1
rs4822983
CHEK2
0.925 0.080 22 28719078 intron variant C/T snv 0.33 1
rs7242481
ELP2 ; SLC39A6
0.925 0.080 18 36129254 5 prime UTR variant G/A snv 0.35 1
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 10
rs4299376
LOC102725159 ; ABCG8
0.851 0.120 2 43845437 intron variant G/C;T snv 6
rs2285947
DNAH11
0.807 0.120 7 21544470 intron variant G/A snv 0.44 1
rs987525
CCDC26
0.807 0.160 8 128933908 intron variant C/A snv 0.31 1
rs16891982
SLC45A2
0.776 0.200 5 33951588 missense variant C/A;G snv 0.65 3
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs11206510 0.763 0.240 1 55030366 intergenic variant T/A;C;G snv 7
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 6
rs8067378 0.752 0.240 17 39895095 regulatory region variant A/G snv 0.50 6
rs2494938
LRFN2
0.752 0.240 6 40568389 intron variant G/A snv 0.51 1
rs3846662
HMGCR
0.763 0.280 5 75355259 non coding transcript exon variant A/G snv 0.50 0.58 5
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 4