Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs786202724
MET
0.925 0.120 7 116777403 missense variant G/A snv 7.0E-06 5
rs121913245
MET
0.925 0.120 7 116783420 missense variant T/C snv 3
rs876658923
EPM2AIP1 ; MLH1
1.000 0.120 3 36993593 frameshift variant TGAACCG/- delins 3
rs121913480
FGFR3
1.000 0.120 4 1806604 missense variant G/T snv 2
rs1383461329
KMT5A
1.000 0.120 12 123389469 missense variant C/T snv 1.4E-05 2
rs1057519736
IDH2
0.752 0.160 15 90088605 missense variant C/G snv 13
rs577715207
TP63
0.827 0.160 3 189886413 missense variant T/A;C snv 4.0E-06; 4.0E-06 7.0E-06 8
rs121913671
MET
0.882 0.160 7 116783353 missense variant G/A;C snv 4
rs267607906
MLH1
1.000 0.160 3 37050576 stop gained A/C;G;T snv 4
rs6886
CAPG
0.925 0.160 2 85394936 missense variant T/A;C snv 0.58 4
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 17
rs56391007
MET
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03 16
rs587779333
PMS2 ; AIMP2
0.851 0.200 7 6009019 start lost T/A;C;G snv 4.0E-06; 2.8E-05 10
rs267607911
MSH2
0.851 0.200 2 47403192 start lost A/C;G;T snv 5.1E-05; 1.4E-05 8
rs587778967
EPM2AIP1 ; MLH1
0.925 0.200 3 36993548 start lost A/C;G snv 8
rs121913246
MET
0.827 0.200 7 116783360 missense variant A/G snv 7
rs1057520039
STK11
0.882 0.200 19 1207169 stop gained C/G;T snv 4
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 23
rs372043866
ERBB2
0.732 0.240 17 39727965 missense variant G/A;C;T snv 3.2E-05; 2.4E-05; 1.2E-05 18
rs28931615
FGFR3
0.732 0.240 4 1804426 missense variant C/A;T snv 13
rs121913484
FGFR3
0.851 0.240 4 1804365 missense variant A/T snv 5
rs1400966919
FGFR4
0.925 0.240 5 177096737 missense variant G/A snv 1.4E-05 3
rs121913412
CTNNB1
0.724 0.280 3 41224633 missense variant A/C;G;T snv 19
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 14
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 44