Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11568818
MMP7
0.763 0.280 11 102530930 upstream gene variant T/A;C snv 2
rs3850699
LOC105378460 ; TRIM8
0.925 0.080 10 102654464 non coding transcript exon variant A/G snv 0.32 2
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 2
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 1
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 2
rs636291
PEX14
0.925 0.080 1 10496040 intron variant G/A snv 0.55 1
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 25
rs817826 0.925 0.080 9 107394019 intergenic variant C/T snv 0.81 2
rs768362387
ATM
0.851 0.360 11 108253846 stop gained C/A snv 3
rs758081262
ATM
0.851 0.360 11 108267258 stop gained C/T snv 1.2E-05 2
rs1800057
ATM
0.776 0.200 11 108272729 missense variant C/A;G snv 1.7E-02 4
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 3
rs2273669
ARMC2
0.925 0.080 6 108963986 intron variant A/G snv 0.19 2
rs11102001
GSTM5 ; EPS8L3
0.925 0.080 1 109757069 missense variant G/A snv 9.4E-02 0.16 2
rs2301241
TXN
0.827 0.160 9 110257228 upstream gene variant G/A;T snv 1
rs387906417
MXI1
1.000 0.080 10 110279296 splice donor variant T/C snv 1
rs137852603
MXI1
1.000 0.080 10 110280017 missense variant A/C snv 1
rs1143627
IL1B
0.605 0.760 2 112836810 5 prime UTR variant G/A snv 0.56 2
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 1
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 10
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 19
rs12255372
TCF7L2
0.667 0.480 10 113049143 intron variant G/A;T snv 3
rs2185710
LOC107986636
1.000 0.080 6 113055846 intron variant A/G snv 0.51 1
rs7611694
SIDT1
0.925 0.080 3 113556777 intron variant A/C;T snv 2
rs1270884 0.925 0.080 12 114247766 intergenic variant A/G snv 0.63 2