Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs2234922
EPHX1
0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs4646903
CYP1A1
0.630 0.640 15 74719300 downstream gene variant A/G;T snv 0.18 36
rs246079
UNG
0.790 0.120 12 109109255 intron variant A/G;T snv 9
rs2014300
RUNX1
0.851 0.080 21 34985564 intron variant A/G;T snv 0.75 5
rs312986 0.925 0.080 18 1898710 intron variant A/G;T snv 3
rs10274928
JAZF1
7 28102469 intron variant A/G;T snv 2
rs2409764
FAM167A ; FAM167A-AS1
8 11423764 3 prime UTR variant A/G;T snv 1
rs26704
PDE4D
5 59237827 intron variant A/G;T snv 1
rs115510139
COL6A3
0.827 0.120 2 237331726 intron variant A/T snv 0.60 6
rs10058728
CSNK1A1
1.000 0.080 5 149524529 intron variant A/T snv 0.64 2
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs1321311 0.742 0.160 6 36655123 regulatory region variant C/A snv 0.28 15
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17 7
rs17761864
SMG6
1.000 0.040 17 2268343 intron variant C/A snv 0.28 2
rs1548418
STEAP1B
7 22685795 intron variant C/A snv 0.89 1
rs2349073
FLACC1
2 201322263 intron variant C/A snv 0.75 1
rs6140125
SLC52A3
20 764903 intron variant C/A snv 1.5E-02 1
rs9288318
FLACC1
2 201331340 intron variant C/A snv 0.63 1
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs3212986
CD3EAP ; ERCC1
0.620 0.400 19 45409478 stop gained C/A;G;T snv 0.29; 4.3E-06; 4.3E-06 42
rs121912657
TP53
0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 24
rs3176352
CDKN1A
0.807 0.120 6 36684562 intron variant C/A;G;T snv 8.0E-06; 0.37; 2.0E-05 7
rs4503732 15 46350065 intron variant C/A;G;T snv 0.92 1
rs1799793
ERCC2
0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72