Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs944289 0.742 0.200 14 36180040 upstream gene variant C/T snv 0.45 16
rs116909374 0.776 0.120 14 36269155 regulatory region variant C/T snv 2.3E-02 11
rs13293512 0.763 0.360 9 94167461 intron variant T/C snv 0.24 11
rs4733616 0.882 0.120 8 127649850 intergenic variant C/A;T snv 3
rs10119760 1.000 0.080 9 97862320 intergenic variant G/C;T snv 1
rs1755787 1.000 0.080 14 36235879 upstream gene variant A/T snv 0.26 1
rs1863347 1.000 0.080 14 36242363 intergenic variant G/A snv 0.77 1
rs2352326 1.000 0.080 X 91591642 intergenic variant T/C snv 1
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs747894155
ADRA1A
1.000 0.080 8 26770171 missense variant C/A;T snv 4.6E-06 1
rs765069734
ADRA2B
1.000 0.080 2 96115436 synonymous variant G/A;C snv 8.1E-06 1
rs79402775
ATF2 ; MIR933
0.827 0.200 2 175167648 mature miRNA variant G/A;T snv 4.4E-02; 1.0E-05 5
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs609429
ATM ; C11orf65
1.000 0.080 11 108325782 intron variant G/C;T snv 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913364
BRAF
0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 34
rs121913227
BRAF
0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs121913375
BRAF
0.851 0.240 7 140753339 missense variant G/A;C snv 7
rs3748093
BRAF
0.925 0.120 7 140800651 intron variant T/A snv 1.5E-02 4
rs11762469
BRAF
1.000 0.080 7 140914412 intron variant A/G;T snv 2
rs1267636
BRAF
1.000 0.080 7 140792239 intron variant T/C snv 0.11 1
rs17161747
BRAF
1.000 0.080 7 140858940 intron variant G/C snv 5.5E-02 1
rs17623204
BRAF
1.000 0.080 7 140806604 intron variant T/A snv 5.5E-02 1
rs6464149
BRAF ; LOC105375536
1.000 0.080 7 140926036 upstream gene variant A/C snv 0.12 1