Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs121913483
FGFR3
0.649 0.560 4 1801841 missense variant C/A;G;T snv 4.2E-06; 1.3E-05 31
rs121913400
CTNNB1
0.683 0.360 3 41224610 missense variant C/A;G;T snv 26
rs78311289
FGFR3
0.689 0.440 4 1806162 missense variant A/C;G snv 4.0E-06 25
rs121913403
CTNNB1
0.683 0.240 3 41224622 missense variant C/A;G;T snv 23
rs730882025
TP53
0.724 0.360 17 7674885 missense variant C/A;G;T snv 21
rs121913412
CTNNB1
0.724 0.280 3 41224633 missense variant A/C;G;T snv 19
rs121913485
FGFR3
0.716 0.400 4 1804372 missense variant A/G snv 18
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
rs2077647
ESR1
0.732 0.320 6 151807942 synonymous variant T/A;C snv 8.1E-06; 0.46 16
rs2229080
DCC
0.742 0.320 18 52906232 missense variant C/A;G snv 0.45 16
rs869320694
FGFR1
0.742 0.520 8 38414790 missense variant T/C snv 16
rs1057519883
CDKN2A
0.742 0.280 9 21971120 missense variant C/G;T snv 14
rs1057519736
IDH2
0.752 0.160 15 90088605 missense variant C/G snv 13
rs1060503115
PMS2
0.763 0.400 7 5978664 missense variant T/A;G snv 13
rs28931615
FGFR3
0.732 0.240 4 1804426 missense variant C/A;T snv 13
rs1057519855
HRAS ; LRRC56
0.776 0.120 11 533873 missense variant CT/AC;TC mnv 11
rs1057519824
MET
0.807 0.120 7 116783374 missense variant T/G snv 10
rs587779333
PMS2 ; AIMP2
0.851 0.200 7 6009019 start lost T/A;C;G snv 4.0E-06; 2.8E-05 10
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs796065354
ESR1
0.882 0.080 6 151944320 missense variant A/G snv 9
rs917411291
GZMM
0.851 0.360 19 544072 start lost A/C;G snv 9
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