Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2981579
FGFR2
0.776 0.280 10 121577821 intron variant A/G snv 0.53 8
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs735665
GRAMD1B
0.776 0.280 11 123490689 intron variant G/A snv 0.15 8
rs4962416
CTBP2
0.882 0.160 10 125008303 intron variant T/C snv 0.23 3
rs3216733
HSPA5 ; LOC107987127
0.882 0.240 9 125241510 upstream gene variant CC/-;C;CCC;CCCC delins 3
rs1016343
PCAT2 ; PCAT1 ; PRNCR1 ; CASC19
0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20 8
rs16901979
PCAT1 ; CASC19
0.724 0.480 8 127112671 intron variant C/A snv 0.16 17
rs2456449
CASC19 ; PCAT1
0.827 0.280 8 127180736 intron variant A/G snv 0.30 5
rs2180341
RNF146
0.882 0.160 6 127279485 intron variant G/A snv 0.73 3
rs16902094
CASC21 ; PCAT1 ; CASC8
0.882 0.160 8 127308101 intron variant A/G snv 0.15 3
rs445114
CASC21 ; PCAT1 ; CASC8
0.882 0.160 8 127310936 intron variant T/A;C snv 3
rs13281615
CASC8 ; POU5F1B ; PCAT1 ; CASC21
0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs7014346
CASC8 ; POU5F1B ; PCAT1
0.732 0.240 8 127412547 intron variant A/G snv 0.63 14
rs1447295
CASC8
0.658 0.400 8 127472793 intron variant A/C;T snv 29
rs4242382 0.763 0.240 8 127505328 intergenic variant A/G;T snv 9
rs4242384 0.882 0.160 8 127506309 regulatory region variant C/A snv 0.88 3
rs9642880
CASC11
0.776 0.240 8 127705823 intron variant G/A;T snv 9
rs4645948
MYC ; CASC11
0.882 0.160 8 127736252 synonymous variant C/T snv 2.8E-02 3
rs2071346
MYC ; CASC11
0.925 0.160 8 127736777 intron variant G/T snv 7.1E-02 3
rs10934853
EEFSEC
0.882 0.160 3 128319530 intron variant C/A snv 0.43 3
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs2853676
TERT
0.667 0.560 5 1288432 intron variant T/A;C snv 29