Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121908735
ADA
0.882 0.160 20 44625581 missense variant G/A snv 1.4E-05 3
rs121908721
ADA ; PKIG
0.882 0.160 20 44621121 missense variant G/A;C snv 2.4E-05 3
rs121908714
ADA
0.925 0.160 20 44626516 missense variant C/A;G;T snv 4.0E-06; 8.0E-06 2
rs121908739
ADA
0.925 0.160 20 44626498 missense variant A/G snv 7.2E-05 7.0E-05 2
rs199422328
ADA
0.925 0.160 20 44626597 missense variant C/A snv 8.0E-06 8.4E-05 2
rs387906267
ADA
0.925 0.160 20 44626601 splice acceptor variant T/C snv 2
rs761242509
ADA
0.925 0.160 20 44625568 splice donor variant C/T snv 2.1E-05 2.8E-05 2
rs121908715
ADA ; PKIG
0.882 0.240 20 44620391 missense variant G/A snv 5.2E-05 2.0E-04 2
rs121908716
ADA ; PKIG
0.925 0.160 20 44623053 missense variant C/T snv 7.2E-05 9.8E-05 2
rs121908723
PKIG ; ADA
0.851 0.240 20 44623039 missense variant C/T snv 1.2E-05 5.6E-05 2
rs121908724
ADA
0.925 0.160 20 44636264 missense variant C/T snv 7.0E-06 1
rs121908726
ADA
0.851 0.160 20 44626570 missense variant G/C;T snv 4.0E-06 1
rs121908727
ADA
0.851 0.160 20 44624272 missense variant G/T snv 1.2E-05 1
rs587776534
ADA
1.000 0.160 20 44651574 splice donor variant C/G snv 1
rs199422327
ADA ; PKIG
1.000 0.160 20 44621082 missense variant A/C snv 4.4E-05 2.1E-05 1