Disease: Neoplasms
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10053538
HAVCR2
0.807 0.160 5 157110499 intron variant C/A;T snv 7
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs1012477
PER3
0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs10235235
ZNF394 ; ZNF789
0.925 0.080 7 99478208 intron variant T/C snv 0.13 4
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs10757278
CDKN2B-AS1
0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10838524
CRY2
0.851 0.120 11 45848626 intron variant A/G snv 0.42 5
rs11141901
DAPK1
0.925 0.080 9 87575750 intron variant A/G snv 0.28 3
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 9
rs114729114
BRAF
0.925 0.080 7 140910797 intron variant C/T snv 1.1E-02 3
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs12922061
CASC16
0.925 0.080 16 52601088 intron variant C/T snv 0.19 3
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs13283662
UHRF2
0.925 0.080 9 6428530 intron variant T/C snv 4
rs1412125
HMGB1
0.724 0.360 13 30467458 intron variant C/G;T snv 17
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs16917302
ZNF365
0.851 0.080 10 62501439 intron variant A/C snv 0.18 5
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs17227210
RUNX1
0.925 0.080 21 35051694 intron variant C/T snv 0.11 3
rs17251221
CASR
0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78