Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs2995264
STN1
0.851 0.080 10 103909085 intron variant G/A snv 0.88 4
rs10739221
LINC01505
0.851 0.080 9 106298549 intron variant T/C;G snv 5
rs1484375
LINC01505
0.882 0.080 9 106305280 intron variant A/G;T snv 3
rs7041168 0.882 0.080 9 107936435 intergenic variant G/A;T snv 3
rs10816595 0.851 0.080 9 107947454 regulatory region variant A/G snv 0.33 4
rs73008229
C11orf65 ; ATM
0.882 0.080 11 108316962 intron variant G/A snv 0.11 3
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs587777894
MTOR
0.776 0.240 1 11124516 missense variant G/A;T snv 9
rs1057519917
MTOR
0.807 0.160 1 11124517 missense variant A/G;T snv 7
rs2234663
IL1RN
0.716 0.480 2 113130529 intron variant ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC/-;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC;ATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGCATCCTGGGGAAAGTGAGGGAAATATGGACATCACATGGAACAACATCCAGGAGACTCAGGCCTCTAGGAGTAACTGGGTAGTGTGC delins 14
rs2153977
MAGI3
0.807 0.240 1 113537449 intron variant C/T snv 0.28 6
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 26
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 26
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 19
rs121913237
NRAS
0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913250
NRAS
0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs4731207
GPR37
0.882 0.080 7 124756591 intron variant G/A snv 0.47 3
rs763733111
PPP6C
0.925 0.120 9 125149801 missense variant G/A snv 4.0E-06 2
rs80338796
RAF1
0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 37
rs1057519918
CASC11 ; MYC
0.851 0.200 8 127738390 missense variant C/T snv 5
rs750664148
CASC11 ; MYC
0.851 0.200 8 127738434 missense variant A/C;G snv 5
rs756091827
MYC ; CASC11
0.851 0.200 8 127738435 missense variant C/G;T snv 6
rs7944031
TEAD1
0.925 0.080 11 12907573 intron variant A/G snv 0.21 2