Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1060501017
FBN1
0.925 0.160 15 48505136 missense variant A/C;G snv 2
rs1060501021
FBN1
0.925 0.160 15 48494210 missense variant A/G snv 2
rs1060501022
FBN1
0.925 0.160 15 48496214 missense variant A/G snv 2
rs1060501023
FBN1
0.925 0.160 15 48430758 stop gained G/A snv 2
rs1060501029
FBN1
0.925 0.160 15 48446909 intron variant T/C snv 2
rs1060501033
FBN1
0.925 0.160 15 48411045 frameshift variant A/- del 2
rs1060501036
FBN1
0.925 0.160 15 48513599 missense variant C/A;G snv 2
rs1060501055
FBN1
0.925 0.160 15 48421997 missense variant A/C snv 2
rs1060501060
FBN1
0.925 0.160 15 48425401 frameshift variant T/- del 2
rs1060501067
FBN1
0.925 0.160 15 48415705 frameshift variant -/C delins 2
rs1060501073
FBN1
0.925 0.160 15 48513612 missense variant C/A snv 2
rs1060501078
FBN1
0.925 0.160 15 48505070 missense variant A/G;T snv 2
rs1060501082
FBN1
0.925 0.160 15 48503811 stop gained G/A snv 2
rs1060501087
FBN1
0.925 0.160 15 48446774 missense variant T/C snv 2
rs1060501093
FBN1
0.925 0.160 15 48425491 missense variant T/C snv 2
rs1064793636
FBN1
0.925 0.160 15 48497290 frameshift variant C/- delins 2
rs1064793637
FBN1
0.925 0.160 15 48526201 frameshift variant T/- delins 2
rs1064793980
FBN1
0.925 0.160 15 48434593 splice donor variant C/G;T snv 2
rs1064794282
FBN1
0.925 0.160 15 48497316 missense variant C/T snv 2
rs1085307531
FBN1
0.925 0.160 15 48444585 missense variant C/T snv 2
rs111231312
FBN1
0.925 0.160 15 48468070 stop gained G/A snv 2
rs111687884
FBN1
0.925 0.160 15 48537704 stop gained G/A;C snv 1.6E-05 2
rs112196241
FBN1
0.925 0.160 15 48415605 missense variant T/C snv 2
rs112375043
FBN1
0.925 0.160 15 48472594 stop gained G/A;C;T snv 3.6E-05 1.4E-05 2
rs112645512
FBN1
0.925 0.160 15 48516225 stop gained G/A snv 2