Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3765524
PLCE1
0.724 0.320 10 94298541 missense variant C/T snv 0.27 0.31 17
rs2064836 1.000 0.080 X 92628018 downstream gene variant A/G;T snv 1
rs405 1.000 0.080 7 91917013 intergenic variant G/A;C;T snv 1
rs7963551
RAD52
0.807 0.160 12 912349 3 prime UTR variant T/G snv 0.13 7
rs10272859
CDK14
0.925 0.120 7 90689160 intron variant G/C snv 0.39 4
rs11632348
IDH2-DT
1.000 0.080 15 90104814 intron variant C/A snv 0.45 1
rs1057519906
IDH2
0.882 0.120 15 90088607 missense variant T/A;C snv 8
rs121913503
IDH2
0.689 0.200 15 90088606 missense variant C/A;T snv 23
rs1805794
NBN
0.605 0.600 8 89978251 missense variant C/G snv 0.35 0.31 41
rs709816
NBN
0.752 0.320 8 89955483 synonymous variant A/G snv 0.47 0.51 10
rs2735383
OSGIN2 ; NBN
0.708 0.360 8 89935041 3 prime UTR variant C/G snv 0.31 18
rs8013403
EFCAB11
1.000 0.080 14 89818395 intron variant A/G snv 0.27 1
rs1800682
ACTA2 ; FAS
0.637 0.440 10 88990206 non coding transcript exon variant A/G snv 0.54 32
rs584368 1.000 0.080 11 88232053 regulatory region variant C/T snv 0.70 1
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs1545224
FABP1
0.925 0.120 2 88124297 3 prime UTR variant A/G snv 0.18 2
rs2853744
SPP1
0.882 0.200 4 87975096 non coding transcript exon variant G/T snv 0.14 4
rs2299939
PTEN
0.827 0.080 10 87897393 intron variant C/A;T snv 5
rs1234220
PTEN
0.851 0.080 10 87885716 intron variant A/G snv 9.1E-02 4
rs1128503
ABCB1
0.564 0.760 7 87550285 synonymous variant A/G snv 0.54 0.63 64
rs201159898
ABCB1
1.000 0.080 7 87549509 missense variant T/A;C snv 1.2E-05 4.9E-05 1
rs749574370
ABCB1
0.925 0.080 7 87545934 missense variant T/A;G snv 4.0E-06; 4.0E-06 2
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs28364274
ABCB1
1.000 0.080 7 87504335 missense variant C/T snv 4.7E-03 4.6E-03 1
rs45456698
ABCB1
1.000 0.080 7 87504335 missense variant C/T snv 1