Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587778967
EPM2AIP1 ; MLH1
0.925 0.200 3 36993548 start lost A/C;G snv 3
rs28931615
FGFR3
0.732 0.240 4 1804426 missense variant C/A;T snv 3
rs121913245
MET
0.925 0.120 7 116783420 missense variant T/C snv 3
rs121913671
MET
0.882 0.160 7 116783353 missense variant G/A;C snv 3
rs267607906
MLH1
1.000 0.160 3 37050576 stop gained A/C;G;T snv 3
rs351855
FGFR4
0.597 0.560 5 177093242 missense variant G/A snv 0.33 0.26 4
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 4
rs121913484
FGFR3
0.851 0.240 4 1804365 missense variant A/T snv 5
rs121913246
MET
0.827 0.200 7 116783360 missense variant A/G snv 5
rs786202724
MET
0.925 0.120 7 116777403 missense variant G/A snv 7.0E-06 5
rs587779333
PMS2 ; AIMP2
0.851 0.200 7 6009019 start lost T/A;C;G snv 4.0E-06; 2.8E-05 5
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 5
rs869320694
FGFR1
0.742 0.520 8 38414790 missense variant T/C snv 7
rs121912664
TP53
0.630 0.320 17 7670699 missense variant C/A;G;T snv 1.2E-05 7
rs121913485
FGFR3
0.716 0.400 4 1804372 missense variant A/G snv 9
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 10
rs121913412
CTNNB1
0.724 0.280 3 41224633 missense variant A/C;G;T snv 10
rs78311289
FGFR3
0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 11
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 12
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 13
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 14
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 14
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 16
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 17
rs121913233
HRAS ; LRRC56
0.627 0.520 11 533874 missense variant T/A;C;G snv 21