Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11671784
MIR24-2 ; LOC284454 ; MIR23A ; MIR27A
0.790 0.240 19 13836482 non coding transcript exon variant G/A snv 1.2E-02 1.2E-02 9
rs56391007
MET
0.752 0.200 7 116771936 missense variant C/T snv 7.9E-03 9.0E-03 16
rs78768932
PXN
0.882 0.080 12 120222977 missense variant C/G;T snv 5.4E-03 5.4E-03 6
rs141613848
SLC9A3R1
0.925 0.080 17 74768481 missense variant A/T snv 1.0E-03 1.2E-03 4
rs3918252
MMP9
20 46010492 missense variant C/G snv 3.6E-05 2.4E-04 1
rs80338948
GJB2
0.763 0.280 13 20189155 missense variant G/A snv 1.2E-04 2.0E-04 12
rs377767426
RET
1.000 0.080 10 43119694 missense variant C/G snv 1.8E-04 1.0E-04 2
rs771086543
FBXL15 ; CUEDC2
10 102422814 missense variant G/A snv 1.3E-04 1.0E-04 1
rs374733251
MET
0.882 0.080 7 116740993 missense variant A/G snv 6.0E-05 7.7E-05 5
rs121917887
NME1-NME2 ; NME1
0.790 0.120 17 51161744 missense variant A/G snv 6.0E-05 7.0E-05 10
rs121434569
EGFR-AS1 ; EGFR
0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs750802459
CASP3
1.000 0.120 4 184635342 frameshift variant TCAGGATAATCCATTTTATAACTGTTGTCCAGGGATATTCCAGAGTC/- delins 5.6E-05 2
rs138281457
GRAP2
22 39955861 missense variant A/G snv 4.0E-06 3.5E-05 1
rs777009146
CTNND1 ; TMX2-CTNND1
11 57805955 missense variant G/A snv 2.0E-05 2.8E-05 1
rs201701502
DDR2
0.851 0.080 1 162775837 missense variant C/G;T snv 1.5E-04 2.1E-05 5
rs377444977
EGFR
0.882 0.080 7 55143443 missense variant G/A snv 5.2E-05 2.1E-05 5
rs765715998
HCK
20 32083944 missense variant G/A snv 2.4E-05 2.1E-05 1
rs757786591
WNT10A
2 218890134 missense variant G/A snv 4.4E-05 2.1E-05 1
rs1156560901
CDK15
2 201880120 missense variant A/G snv 1.4E-05 2
rs760101437
EGFR
0.851 0.160 7 55154018 missense variant G/A snv 3.2E-05 1.4E-05 6
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs1213469537
CAV1
0.882 0.080 7 116559145 missense variant C/T snv 4.0E-06 1.4E-05 9
rs770795658
PGR ; PGR-AS1
11 101127788 missense variant C/T snv 6.1E-06 7.0E-06 1
rs757816355
KRAS
12 25225657 missense variant C/T snv 1.2E-05 7.0E-06 1
rs1451539938
CD82
0.925 0.080 11 44618361 missense variant A/G snv 4.1E-06 7.0E-06 3