Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs1011970
CDKN2B-AS1
0.677 0.320 9 22062135 intron variant G/T snv 0.23 22
rs11200014
FGFR2
0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 19
rs4808075
BABAM1 ; USHBP1
0.701 0.280 19 17279482 intron variant T/C snv 0.26 18
rs11119608
KCNH1
0.708 0.280 1 210816167 intron variant T/G snv 0.21 17
rs11168936
TUBA1C
0.708 0.280 12 49251457 intron variant T/A;C snv 17
rs115392158
HLA-B
0.708 0.280 6 31347004 intron variant A/G snv 17
rs11571818
BRCA2
0.708 0.280 13 32394673 intron variant T/C snv 6.6E-03 6.0E-03 17
rs11844632
RAD51B
0.708 0.280 14 68559662 intron variant G/A snv 0.23 17
rs12601991
HNF1B
0.708 0.280 17 37741642 intron variant T/A;G snv 17
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs2300206
RALY
0.708 0.280 20 34002002 intron variant G/C;T snv 17
rs481519
NEK10
0.708 0.280 3 27285723 intron variant C/A;T snv 17
rs56404467
FRY
0.708 0.280 13 32265853 intron variant G/A snv 1.3E-02 17
rs73110464
KRT8
0.708 0.280 12 52918828 intron variant C/T snv 0.12 17
rs7725218
TERT
0.708 0.280 5 1282299 intron variant G/A snv 0.38 17
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs11651755
HNF1B
0.763 0.160 17 37739849 intron variant T/C snv 0.52 9
rs7405776
HNF1B
0.807 0.120 17 37733029 intron variant G/A;C snv 6
rs1400482
LINC00824
0.925 0.120 8 128529685 intron variant G/A snv 0.13 2
rs144962376
MLLT10
0.925 0.120 10 21589903 intron variant CCCCTT/-;CCCCTTCCCCTT delins 2
rs1879586
PLEKHM1
0.925 0.120 17 45489971 intron variant C/G snv 0.12 2
rs2165109
MIR4435-2HG ; ACOXL
0.925 0.120 2 111061081 intron variant A/C snv 0.25 2