Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs1023835002
B2M ; PATL2
0.763 0.280 15 44711547 start lost A/G;T snv 10
rs1042522
TP53
0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs10519097
RORA
0.708 0.320 15 60997989 intron variant C/T snv 0.13 18
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057519877
B2M ; PATL2
0.763 0.280 15 44711549 start lost G/A snv 10
rs1057519879
PATL2 ; B2M
0.763 0.280 15 44711548 start lost T/C;G snv 10
rs1057519894
EZH2
0.925 0.160 7 148811650 missense variant T/A;G snv 2
rs1057519909
MAP2K1
0.790 0.240 15 66435116 missense variant A/C snv 7
rs1057519918
CASC11 ; MYC
0.851 0.200 8 127738390 missense variant C/T snv 5
rs1057519941
PIK3CA
0.776 0.240 3 179203761 missense variant T/C;G snv 10
rs1057519942
PIK3CA
0.724 0.320 3 179203760 missense variant G/A snv 16
rs1057519952
RHOA
0.882 0.160 3 49375577 missense variant G/A snv 5
rs1057519953
RHOA
0.807 0.200 3 49375576 missense variant C/A;T snv 8
rs1057519954
RHOA
0.882 0.160 3 49375465 missense variant T/A;C;G snv 4
rs1057520001
TP53
0.677 0.360 17 7674886 missense variant A/C;G snv 23
rs1057520002
TP53
0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs1057520007
TP53
0.701 0.440 17 7674917 missense variant T/A;C;G snv 21
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11943456
TMEM165
0.708 0.320 4 55410167 intron variant T/C snv 0.42 18
rs121434595
NRAS
0.708 0.320 1 114716124 missense variant C/A;G;T snv 19
rs121434596
NRAS
0.677 0.440 1 114716123 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 26
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121908689
RAD54L ; LRRC41
0.925 0.120 1 46272758 missense variant T/A snv 2