Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs140598
FBN1
0.827 0.160 15 48487333 missense variant G/A;C snv 3.2E-02 5
rs1057519320
FBN1
0.807 0.160 15 48444574 missense variant G/A snv 4
rs137854468
FBN1
0.851 0.160 15 48487396 missense variant C/T snv 4
rs61746008
FBN1
0.882 0.160 15 48412619 missense variant G/A;C snv 7.3E-04 3
rs1057520131
FBN1
0.925 0.240 15 48508633 missense variant A/C snv 2
rs137854467
FBN1
0.790 0.280 15 48600217 missense variant G/A snv 2
rs137854478
FBN1
0.851 0.160 15 48488233 missense variant C/T snv 2
rs137854480
FBN1
0.742 0.200 15 48537629 missense variant G/A snv 2
rs137854485
FBN1
0.925 0.160 15 48515402 missense variant G/A snv 2
rs193922185
FBN1
0.752 0.200 15 48505037 missense variant G/A snv 2
rs730880099
FBN1
0.742 0.200 15 48510125 missense variant G/A snv 2
rs794728228
FBN1
0.925 0.160 15 48468064 stop gained G/A snv 2
rs1064793118
FBN1
1.000 0.160 15 48437038 missense variant C/T snv 1
rs1085307528
FBN1
1.000 0.160 15 48508666 missense variant C/T snv 1
rs113393517
FBN1
1.000 0.160 15 48481660 missense variant C/A;G snv 1
rs113422242
FBN1
0.763 0.240 15 48510065 stop gained G/A snv 7.0E-06 1
rs137854461
FBN1
0.790 0.280 15 48437026 missense variant T/C snv 1
rs137854462
FBN1
1.000 0.160 15 48510115 missense variant T/A snv 1
rs137854464
FBN1
0.851 0.200 15 48425483 missense variant C/T snv 7.0E-06 1
rs137854475
FBN1
0.882 0.200 15 48487155 missense variant C/T snv 1.3E-03 1.6E-03 1
rs137854479
FBN1
0.925 0.200 15 48497298 missense variant T/C snv 1
rs137854484
FBN1
0.925 0.160 15 48488193 missense variant C/T snv 1
rs25403
FBN1
0.882 0.200 15 48613073 missense variant G/A snv 1
rs397514558
FBN1
0.851 0.200 15 48490013 missense variant G/A snv 7.0E-06 1
rs397515812
FBN1
0.925 0.160 15 48468427 stop gained G/A;C snv 4.0E-06; 4.0E-06 1