Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143046984
LOC105370557 ; PCNX1
0.790 0.080 14 70937529 intron variant -/A delins 4.2E-02 9
rs202110856
ERAP1
0.790 0.080 5 96794169 intron variant -/C delins 2.1E-05 9
rs377429877
STARD13
0.776 0.080 13 33518027 intron variant -/TAA delins 6.0E-02 10
rs727502902
BRAF
0.882 0.080 7 140753338 inframe insertion -/TAG delins 4.0E-06 4
rs121913289
PTEN
1.000 0.080 10 87958013 frameshift variant A/- delins 4
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 18
rs6058093
PIGU
0.776 0.080 20 34625392 intron variant A/C snv 0.55 12
rs1057519939
PIK3CA
0.776 0.160 3 179203763 missense variant A/C snv 10
rs1566734
PTPRJ
0.807 0.120 11 48123823 missense variant A/C snv 0.17 0.15 10
rs9924886
CDH3
0.776 0.080 16 68710036 intron variant A/C snv 0.25 10
rs10911251
LAMC1
0.790 0.080 1 183112059 intron variant A/C snv 0.37 9
rs16973225
LOC102724001
0.790 0.080 15 81937658 intron variant A/C snv 7.4E-02 9
rs2184857
LOC105373224
0.790 0.080 1 239918447 upstream gene variant A/C snv 0.45 9
rs6720296
LINC01121
0.790 0.080 2 45181130 intron variant A/C snv 0.52 9
rs73975588
NXN
0.790 0.080 17 913501 intron variant A/C snv 9.9E-02 9
rs1057519928
PIK3CA
0.807 0.200 3 179221147 missense variant A/C snv 8
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs587780424
PPARG
3 12433975 missense variant A/C snv 1
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs11150038
CLEC3A
0.790 0.080 16 78042662 intron variant A/C;G snv 10
rs17102823 0.776 0.080 14 34894698 intergenic variant A/C;G snv 10
rs281875324
SMAD4
1.000 0.120 18 51065456 missense variant A/C;G snv 3
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs1057519975
TP53
0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 33