Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs371194629
HLA-G
0.790 0.320 6 29830804 3 prime UTR variant -/ATTTGT;ATTTGTTCACGCCT;ATTTGTTCATGCCT ins 8
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1257821596
AVP
1.000 0.040 20 3083027 frameshift variant -/C delins 7.0E-06 1
rs61764370
KRAS
0.662 0.320 12 25207290 3 prime UTR variant A/C snv 6.2E-02 29
rs1057519939
PIK3CA
0.776 0.160 3 179203763 missense variant A/C snv 10
rs1057519987
TP53
0.776 0.280 17 7673810 missense variant A/C snv 10
rs1057519928
PIK3CA
0.807 0.200 3 179221147 missense variant A/C snv 8
rs1057519909
MAP2K1
0.790 0.240 15 66435116 missense variant A/C snv 7
rs3213182
E2F1 ; NECAB3
1.000 0.040 20 33675427 upstream gene variant A/C snv 7.2E-02 1
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057519986
TP53
0.776 0.240 17 7673811 missense variant A/C;G snv 10
rs11016879
MGMT
0.882 0.040 10 129691518 intron variant A/C;G snv 0.66 4
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
rs760043106
TP53
0.645 0.440 17 7674947 missense variant A/C;G;T snv 32
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs1057519747
TP53
0.716 0.280 17 7675094 missense variant A/C;G;T snv 23
rs1057519981
TP53
0.689 0.440 17 7674251 missense variant A/C;G;T snv 22
rs876660821
TP53
0.689 0.400 17 7675075 missense variant A/C;G;T snv 22
rs530941076
TP53
0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 21
rs786203436
TP53
0.701 0.280 17 7675125 missense variant A/C;G;T snv 20
rs1057519927
PIK3CA
0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
rs864622237
TP53
0.716 0.320 17 7674263 missense variant A/C;G;T snv 17
rs967461896
TP53
0.724 0.240 17 7675086 missense variant A/C;G;T snv 17