Disease: Malignant Neoplasms
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10109984
PRKDC
0.925 0.080 8 47891114 intron variant T/C snv 0.54 4
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
rs10204525
PDCD1
0.701 0.440 2 241850169 3 prime UTR variant C/T snv 0.21 20
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1029342144
KLLN ; PTEN
0.882 0.120 10 87864162 5 prime UTR variant C/G;T snv 6
rs1043210477
GPX1
0.701 0.520 3 49358250 missense variant G/A snv 19
rs1044129
AVEN ; RYR3
0.790 0.200 15 33866065 3 prime UTR variant A/G;T snv 9
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057519847
EGFR
0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848
EGFR
0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs1063320
HLA-G
0.752 0.360 6 29830972 3 prime UTR variant C/G;T snv 12
rs10877887
LINC01465 ; MIRLET7I
0.701 0.440 12 62603400 non coding transcript exon variant T/C snv 0.42 18
rs10889677
IL23R
0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs10895068
PGR ; PGR-AS1
0.752 0.240 11 101129483 5 prime UTR variant C/T snv 3.6E-02 14
rs10896449 0.827 0.200 11 69227200 intergenic variant A/G snv 0.53 7
rs11075995
FTO
0.882 0.080 16 53821379 intron variant A/T snv 0.77 5
rs11134527
MIR218-2 ; SLIT3
0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs11225395
MMP8
0.776 0.360 11 102725749 intron variant A/C;G snv 11