Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs4698803
EGF
1.000 0.040 4 109993271 missense variant A/G;T snv 0.85 1
rs6533485
EGF
1.000 0.040 4 110006407 intron variant G/C snv 0.61 1
rs769047429
EGF
1.000 4 109999827 frameshift variant -/G delins 8.0E-06 1
rs771293553
EGF
1.000 0.120 4 109913378 missense variant T/A;C snv 1
rs778040733
EGF
1.000 0.080 4 109988662 missense variant T/C snv 1.2E-05 1.4E-05 1
rs887027
EGF
4 109977659 intron variant C/A;T snv 1
rs887183646
EGF
1.000 0.080 4 109976079 missense variant C/T snv 3.2E-05 2.8E-05 1
rs902596253
EGF
1.000 0.080 4 109941062 missense variant C/T snv 1
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