Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs75076352
RET
0.689 0.240 10 43114500 missense variant T/A;C;G snv 1.2E-05 24
rs77724903
RET
0.672 0.280 10 43118460 missense variant A/G;T snv 4.0E-06; 2.1E-03 23
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs966423
DIRC3
0.776 0.200 2 217445617 intron variant C/G;T snv 11
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs2227869
ERCC5 ; BIVM-ERCC5
0.790 0.240 13 102862735 missense variant G/A;C snv 4.3E-02 9
rs1443438
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv 8
rs763538721
HIF1A-AS3 ; HIF1A
0.807 0.160 14 61740897 missense variant T/A snv 4.0E-06 8
rs778212685
CHEK2
0.827 0.120 22 28712015 missense variant C/A;G;T snv 4.0E-06 8
rs1064795638
BAP1
0.851 0.080 3 52403251 stop gained G/A snv 7
rs1169803481
EGFR
0.807 0.160 7 55198851 missense variant A/G snv 4.0E-06 7
rs121913308
RET
0.827 0.120 10 43114492 missense variant A/C;G;T snv 6
rs35187787
CDH1
0.827 0.120 16 68822063 missense variant G/A;T snv 3.3E-03; 2.4E-05 6
rs6793295
LRRC34
0.827 0.240 3 169800667 missense variant T/C;G snv 0.37; 1.8E-04 6
rs768827923
PIK3CD
0.851 0.080 1 9721816 missense variant T/G snv 6
rs776935407
SGSM3
0.851 0.080 22 40409261 missense variant T/A snv 4.1E-06 6
rs587779826
ATM
0.851 0.360 11 108267344 splice donor variant T/C snv 4.0E-06 5
rs786203472
CHEK2
0.827 0.120 22 28719414 start lost T/C snv 5
rs863224748
CHEK2
0.827 0.120 22 28734721 start lost T/C snv 5
rs1800858
RET
0.851 0.160 10 43100520 synonymous variant A/C;G snv 0.73 4
rs768891111
XRCC3 ; KLC1
0.851 0.080 14 103699474 stop gained C/A;G;T snv 4.0E-06; 4.0E-06 4
rs907580 0.851 0.080 9 97860315 downstream gene variant T/A;C;G snv 4
rs996807218
KIDINS220
0.882 0.080 2 8827045 missense variant T/C snv 4
rs1031583860
GLYAT
0.882 0.080 11 58709815 missense variant T/C snv 3
rs2708896
PKD1L1
0.882 0.080 7 47955186 upstream gene variant T/C;G snv 3