Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs118101777
IDH2
0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 42
rs55819519
TP53
0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs28934575
TP53
0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs28934574
TP53
0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 31
rs1057519903
H3-3A
0.683 0.080 1 226064434 missense variant A/T snv 28
rs6010620
RTEL1 ; RTEL1-TNFRSF6B
0.701 0.360 20 63678486 intron variant A/C;G snv 21
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs760090729
H3C10
0.851 0.040 6 27810468 missense variant G/A snv 4
rs866960721
H3C4
0.851 0.040 6 26196856 missense variant C/G;T snv 4.0E-06 4
rs1415342243
H3C6
0.851 0.040 6 26225549 missense variant G/A snv 4.0E-06 4
rs751859698
MSH4
0.925 0.040 1 75898031 missense variant T/A;C snv 1.2E-05 2