Disease: Non-Small Cell Lung Carcinoma
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1026411
LOC105375751 ; PCAT1
0.827 0.080 8 127014165 intron variant G/A;C snv 0.25 5
rs1046175
PAOX
0.851 0.080 10 133391446 stop gained C/A;G;T snv 1.2E-05; 0.88 4
rs1057519729
MAP2K1
0.827 0.080 15 66435113 missense variant A/C snv 6
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
rs1057519861
EGFR ; EGFR-AS1
0.776 0.080 7 55181398 missense variant T/A snv 15
rs10937405
TP63
0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs11540478
IDH2
0.851 0.080 15 90085305 synonymous variant G/A;C snv 3.5E-02; 6.4E-06 4
rs1171287261
EGFR
0.851 0.080 7 55191839 missense variant G/A snv 4
rs11778573
CCN4
0.851 0.080 8 133216687 intron variant T/G snv 0.59 4
rs1226168728
PPP1R13L
0.851 0.080 19 45398021 missense variant G/C snv 7.0E-06 4
rs1362623672
ERCC1
0.851 0.080 19 45421317 missense variant G/C snv 1.4E-05 4
rs1423493595
UBE2V1 ; TMEM189-UBE2V1
0.851 0.080 20 50082836 missense variant G/A snv 4.0E-06 7.0E-06 5
rs1454694 0.827 0.080 4 181276794 intergenic variant T/C snv 0.20 5
rs1458974438
STK11
0.807 0.080 19 1206957 missense variant G/A snv 9
rs1878022
CMKLR1
0.851 0.080 12 108305255 intron variant C/T snv 0.70 4
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20 6
rs2293347
EGFR
0.851 0.080 7 55201223 synonymous variant C/T snv 0.14 9.5E-02 4
rs2564978
CD55
0.827 0.080 1 207321071 upstream gene variant T/C snv 0.77 6
rs2835267
SETD4 ; LOC100133286
0.827 0.080 21 36074727 intron variant T/C snv 0.63 6
rs2977536
CCN4
0.851 0.080 8 133207034 intron variant G/C snv 0.36 4
rs3805213
NOCT ; ELF2
0.851 0.080 4 139044570 intron variant C/T snv 0.23 4
rs4065
PLAU ; C10orf55
0.851 0.080 10 73916706 3 prime UTR variant C/T snv 0.51 4
rs4488809
TP63
0.827 0.080 3 189638472 intron variant T/C snv 0.45 5
rs4978754
ELP1
0.851 0.080 9 108884801 intron variant T/C snv 0.92 4