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
rs386352318
KCNJ5
0.925 0.080 11 128911776 missense variant T/G snv 4
rs4539
CYP11B2 ; GML
0.925 0.080 8 142915123 missense variant T/C snv 0.42 0.38 4
rs756363791
OGG1
0.882 0.080 3 9756823 missense variant G/A snv 2.0E-05 4
rs2838958
SLC19A1
1.000 0.080 21 45528653 intron variant G/A snv 0.45 3
rs746497256
NFE2L2
0.925 0.080 2 177231925 synonymous variant A/G snv 8.0E-06 7.0E-06 3
rs17503908
ATM ; C11orf65
1.000 0.080 11 108344670 intron variant T/G snv 6.7E-02 2
rs370574590
PCSK9
1.000 0.080 1 55058628 missense variant G/A;T snv 3.2E-05; 1.2E-05 2
rs4952490
SLC8A1-AS1 ; SLC8A1
1.000 0.080 2 40145564 intron variant A/G snv 0.33 2
rs5789
PTGS1
1.000 0.080 9 122381694 missense variant C/A snv 1.8E-02 1.8E-02 2
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs7837328
CASC8 ; PCAT1 ; POU5F1B
0.882 0.120 8 127410882 intron variant A/G snv 0.52 8
rs2302615
ODC1-DT ; SNORA80B ; ODC1
0.807 0.120 2 10448012 intron variant C/T snv 0.31 7
rs1057517457
MUTYH
0.851 0.120 1 45332804 frameshift variant GCCAGCCCAG/- delins 7.0E-06 6
rs10941112
AMACR ; C1QTNF3-AMACR
0.882 0.120 5 34004602 missense variant C/T snv 0.42 0.38 4
rs1268298845
APC
0.882 0.120 5 112780878 missense variant G/A snv 4.0E-06 4
rs2276020
AIP ; MIR6752
1.000 0.120 11 67490085 missense variant C/G;T snv 3.4E-02 2
rs10795668
LOC105376400
0.724 0.160 10 8659256 upstream gene variant G/A snv 0.24 17
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins 11
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
rs2959656
MEN1 ; MAP4K2
0.851 0.160 11 64804546 missense variant T/C snv 0.94 0.90 5
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 17
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 14
rs3842787
PTGS1
0.776 0.200 9 122371228 missense variant C/T snv 5.9E-02 8.5E-02 11