Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519699
PIK3CA
3 179218315 missense variant G/A snv 2
rs1057519740
SMAD4
18 51065532 missense variant C/A snv 1
rs1057519741
SMAD4
18 51078417 missense variant G/T snv 1
rs1057519754
AKT2
19 40236313 missense variant T/C snv 1
rs1057519760
EGFR
7 55160314 missense variant A/G snv 1
rs121913326
APC
5 112839729 stop gained G/T snv 1
rs121913328
APC
5 112839693 stop gained C/T snv 1
rs121913329
APC
5 112839726 stop gained C/T snv 1
rs121913462
APC
5 112839510 stop gained G/A;T snv 1
rs74535574
APC
5 112839879 stop gained C/A;T snv 1
rs869312784
APC
5 112838674 missense variant A/G snv 1
rs11727676
HHIP
0.776 0.080 4 144737912 synonymous variant T/C snv 6.6E-02 6.4E-02 14
rs12916300
HERC2
0.742 0.080 15 28165345 intron variant C/T snv 0.50 13
rs58658771 0.776 0.080 15 32709533 intergenic variant T/A snv 0.20 13
rs10821907 0.776 0.080 10 50888694 upstream gene variant C/T snv 0.20 12
rs4360494
SF3A3
0.776 0.080 1 37990219 upstream gene variant G/C snv 0.45 12
rs6058093
PIGU
0.776 0.080 20 34625392 intron variant A/C snv 0.55 12
rs6584283
LINC01475
0.776 0.080 10 99530544 intron variant T/C snv 0.56 12
rs9470361 0.776 0.080 6 36655602 regulatory region variant G/A;T snv 12
rs1412834
CDKN2B-AS1
0.790 0.080 9 22110132 intron variant T/C snv 0.64 11
rs2179593
TOX2
0.790 0.080 20 44031646 intron variant C/A snv 0.71 11
rs35107139
BMP4
0.776 0.080 14 53952388 intron variant A/C;G;T snv 11
rs35446936
ACTRT3
0.776 0.080 3 169768720 intron variant G/A snv 0.21 11
rs6063514 0.776 0.080 20 50438781 intergenic variant C/T snv 0.42 11
rs10049390
SLCO2A1
0.776 0.080 3 133982275 intron variant G/A snv 0.67 10