Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs1323833193
EGF
0.851 0.160 4 109994859 missense variant C/G snv 4.0E-06 4
rs1436919825
EGF
0.882 0.080 4 109976175 missense variant G/A snv 3
rs2237051
EGF
0.925 0.120 4 109980042 missense variant G/A snv 0.46 0.53 3
rs781754383
EGF
0.882 0.080 4 109960942 missense variant C/A;T snv 8.0E-06; 4.0E-06 3
rs11568943
EGF
0.925 0.080 4 109961965 missense variant G/A snv 9.8E-02 0.12 2
rs11569017
EGF
0.925 0.120 4 109980955 missense variant A/T snv 7.3E-02 5.0E-02 2
rs3756261
EGF
0.925 0.160 4 109911150 upstream gene variant T/C snv 9.9E-02 2
rs7692976
EGF
1.000 0.040 4 109990411 intron variant A/G;T snv 2
rs776728511
EGF
0.925 0.040 4 109945192 missense variant A/G snv 4.0E-06 2
rs10029654
EGF
1.000 0.040 4 109940771 intron variant G/A snv 0.38 1
rs11568835
EGF
1.000 0.120 4 109911514 upstream gene variant G/A snv 2.7E-02 1
rs11568953
EGF
1.000 0.040 4 109963240 synonymous variant A/G snv 9.7E-03 1.0E-02 1
rs11568972
EGF
4 109967851 intron variant A/C snv 0.27 1
rs11569142
EGF
4 110010783 intron variant G/T snv 1.1E-02 1
rs1177684571
EGF
1.000 0.080 4 109976199 missense variant G/C;T snv 4.0E-06 1
rs1185124983
EGF
1.000 0.080 4 109960879 missense variant G/A snv 4.0E-06 1
rs121434567
EGF
1.000 0.160 4 110004540 missense variant C/T snv 1.6E-05 2.8E-05 1
rs1226967393
EGF
4 109969119 missense variant G/A;C snv 4.0E-06 1
rs1336242054
EGF
1.000 0.080 4 109974747 missense variant A/G snv 4.0E-06 1
rs1860129
EGF
4 109965187 intron variant G/C snv 0.55 1
rs2298991
EGF
1.000 0.040 4 109970856 intron variant T/A;G snv 1
rs28629923
EGF
4 109932621 intron variant G/A snv 0.33 1
rs377602035
EGF
4 109937360 intron variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT;TTTTTTT delins 1