Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs121913500
IDH1
0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs1138272
GSTP1
0.611 0.600 11 67586108 missense variant C/T snv 5.9E-02 5.5E-02 42
rs1799969
ICAM1
0.637 0.560 19 10284116 missense variant G/A snv 0.11 9.3E-02 38
rs3761549
FOXP3
0.724 0.480 X 49260888 intron variant G/A snv 9.6E-02 18
rs1799950
BRCA1
0.752 0.240 17 43094464 missense variant T/C snv 4.7E-02 4.6E-02 13
rs80357796
BRCA1
0.752 0.240 17 43094464 frameshift variant T/- del 11
rs63750206
MLH1
0.807 0.200 3 36996701 missense variant G/A;C;T snv 9
rs267608058
FBXO11 ; MSH6
0.851 0.200 2 47800130 frameshift variant TCAG/- delins 7.0E-06 6
rs80359763
BRCA2
0.851 0.240 13 32394864 frameshift variant GT/- delins 5
rs1161136341
HDAC9
0.925 0.080 7 18591621 missense variant G/A snv 8.0E-06 1.4E-05 2
rs774238794
HDAC9
0.925 0.080 7 18644690 missense variant G/A;T snv 4.1E-05; 4.1E-06 2
rs869312780
PTEN
0.925 0.120 10 87957983 frameshift variant AG/- delins 2