Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1535989 0.925 0.080 13 105370372 intergenic variant A/G;T snv 4
rs939481814
UGT1A1 ; UGT1A5 ; UGT1A9 ; UGT1A3 ; UGT1A6 ; UGT1A7 ; UGT1A8 ; UGT1A10 ; UGT1A4
2 233767063 synonymous variant A/T snv 1
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs5789
PTGS1
1.000 0.080 9 122381694 missense variant C/A snv 1.8E-02 1.8E-02 2
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs55819519
TP53
0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs121913409
CTNNB1
0.708 0.400 3 41224646 missense variant C/A;G;T snv 21
rs121912532
STON1-GTF2A1L ; LHCGR ; GTF2A1L
0.776 0.280 2 48688065 missense variant C/A;G;T snv 1.2E-05 12
rs2720574
PDGFRL
8 17578682 intron variant C/A;G;T snv 1
rs775144154
SLC19A1
0.627 0.600 21 45531904 missense variant C/A;T snv 9.7E-06; 1.4E-05 38
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs5277
PACERR ; PTGS2
0.790 0.160 1 186679065 synonymous variant C/G;T snv 0.12; 8.0E-06 9
rs7968585
LINC02354
0.851 0.160 12 47838310 downstream gene variant C/G;T snv 7
rs778826879
MAPK3
16 30121948 missense variant C/G;T snv 1.2E-05; 8.0E-06 3
rs2276020
AIP ; MIR6752
1.000 0.120 11 67490085 missense variant C/G;T snv 3.4E-02 2
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs36053993
MUTYH
0.677 0.280 1 45331556 missense variant C/T snv 3.0E-03 3.3E-03 31
rs3842787
PTGS1
0.776 0.200 9 122371228 missense variant C/T snv 5.9E-02 8.5E-02 11
rs2302615
ODC1-DT ; SNORA80B ; ODC1
0.807 0.120 2 10448012 intron variant C/T snv 0.31 7
rs104894194
AIP
0.925 11 67483198 stop gained C/T snv 2.8E-05 2.1E-05 4
rs10941112
AMACR ; C1QTNF3-AMACR
0.882 0.120 5 34004602 missense variant C/T snv 0.42 0.38 4