Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs62408225
BACH2
1.000 0.120 6 90246690 intron variant A/G snv 0.26 2
rs6543124
IL18R1
1.000 0.120 2 102370999 intron variant T/A snv 0.44 1
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs74767530
CFTR
0.851 0.320 7 117627537 stop gained C/T snv 5.6E-05 4.9E-05 5
rs759412116
ERCC2
0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 55
rs7817
IFRD1
0.925 0.200 7 112475603 3 prime UTR variant C/G;T snv 2
rs8046011 1.000 0.120 16 11226805 downstream gene variant G/A;T snv 3
rs828618
DCBLD2
0.925 0.160 3 98822789 intron variant G/A snv 0.28 0.22 2
rs9268644
HLA-DRA
0.827 0.360 6 32440267 intron variant A/C snv 0.68 5