Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 121
rs763361
CD226
0.689 0.520 18 69864406 missense variant T/A;C snv 4.0E-06; 0.52 21
rs2076530
TSBP1-AS1 ; BTNL2
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 17
rs5844572
MIF ; MIF-AS1
0.752 0.360 22 23893562 intron variant -/ATTC delins 11
rs9277554
HLA-DPB1
0.790 0.520 6 33087761 3 prime UTR variant C/T snv 0.38 7
rs730881997
TP53
0.925 0.200 17 7675999 missense variant A/C;T snv 8.0E-06 4
rs6922466 0.882 0.240 6 138123793 regulatory region variant A/G snv 0.21 3
rs7503953 0.882 0.320 17 6238357 intergenic variant A/C snv 0.81 3
rs42041
CDK6
0.882 0.280 7 92617430 intron variant C/G snv 0.21 3
rs9277341
HLA-DPA1
0.882 0.280 6 33071848 intron variant T/A;C snv 3
rs1949829 0.925 0.200 7 51470190 upstream gene variant C/T snv 0.12 2
rs26595 0.925 0.200 5 116423793 intergenic variant G/A;T snv 2
rs3117242 0.925 0.200 6 33102116 upstream gene variant A/G snv 0.34 2
rs151269264
ACR ; LOC105373100
0.925 0.200 22 50738307 synonymous variant G/A;C snv 1.6E-05; 6.0E-05 2
rs118099717
CDS1
0.925 0.200 4 84604268 missense variant G/C snv 1.2E-03 9.1E-04 2
rs595018
LOC105369322
0.925 0.200 11 60824803 upstream gene variant T/A;C snv 2
rs10548957
RXRB
0.925 0.200 6 33195861 non coding transcript exon variant AG/- delins 2
rs6531
RXRB
0.925 0.200 6 33195674 synonymous variant G/A snv 0.77 0.77 2