Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1051266
SLC19A1
0.627 0.640 21 45537880 missense variant T/C;G snv 0.55; 4.4E-06 41
rs1051753269
EGFR
0.790 0.120 7 55174029 missense variant G/A snv 7.0E-06 7
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1056503
XRCC4
0.851 0.200 5 83353158 synonymous variant T/A;G snv 4.0E-06; 0.23 4
rs1057519698
ALK
0.827 0.120 2 29222347 missense variant A/G;T snv 8
rs1057519729
MAP2K1
0.827 0.080 15 66435113 missense variant A/C snv 6
rs1057519781
ALK
0.807 0.160 2 29209816 missense variant C/G snv 9
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
rs1057519788
ROS1
0.925 0.080 6 117317184 missense variant C/T snv 6
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
rs1057519858
STK11
1.000 0.080 19 1220495 missense variant G/T snv 1
rs1057519861
EGFR ; EGFR-AS1
0.776 0.080 7 55181398 missense variant T/A snv 15
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs1057523347
TP53
0.925 0.160 17 7673789 stop gained A/G;T snv 2
rs1059292
SLC3A2 ; SNORD29 ; SNORD25 ; SNHG1 ; SNORD30 ; SNORD28 ; SNORD27 ; SNORD26
1.000 0.080 11 62855579 non coding transcript exon variant T/C snv 7.2E-02 9.0E-02 1
rs1060501205
TP53
0.827 0.120 17 7673749 missense variant TG/GT mnv 5
rs1060503460
NBN
0.925 0.200 8 89955461 missense variant A/T snv 2
rs1061302
NBN
0.827 0.160 8 89946194 synonymous variant T/C snv 0.35 0.30 5
rs1061622
TNFRSF1B
0.633 0.760 1 12192898 missense variant T/G snv 0.22 0.22 33
rs1061624
TNFRSF1B
0.776 0.320 1 12207208 3 prime UTR variant A/G snv 0.48 8
rs10680577
RAB4B-EGLN2 ; EGLN2
0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26