Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1948915
PCAT1 ; CASC19 ; CCAT1
1.000 0.160 8 127210176 intron variant T/C snv 0.43 1
rs2242652
TERT
0.724 0.400 5 1279913 intron variant G/A snv 0.18 16
rs2720680
PVT1
0.851 0.160 8 128102971 intron variant A/G snv 0.33 4
rs11715604
NCK1
0.851 0.160 3 136870707 intron variant A/G;T snv 4
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 12
rs397507483
BRAF
0.790 0.400 7 140753348 missense variant C/A;T snv 13
rs121913361
BRAF
0.807 0.280 7 140753349 missense variant C/A;G;T snv 7
rs121913338
BRAF
0.677 0.400 7 140753354 missense variant T/A;C;G snv 24
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs1057519718
BRAF
0.925 0.160 7 140753355 missense variant CA/TC mnv 2
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 10
rs180177040
BRAF
0.790 0.360 7 140754187 missense variant T/C;G snv 9
rs121913355
BRAF
0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs121913351
BRAF
0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs756168629
LRP1B
1.000 0.160 2 140841050 missense variant C/T snv 4.8E-05 1.4E-05 2
rs61070260
LRP1B
1.000 0.160 2 140846426 intron variant G/A snv 5.7E-02 1
rs75002266
ORC4
0.827 0.160 2 147939241 missense variant G/A snv 3.2E-03 3.0E-03 6
rs12374648
LOC102723831
1.000 0.160 6 151208234 intron variant A/G snv 0.22 1
rs7781265
SMARCD3
1.000 0.160 7 151253854 intron variant G/A snv 0.16 1
rs34229995 1.000 0.160 6 15243787 upstream gene variant C/G snv 2.1E-02 1