Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057518912
FBN1
1.000 0.160 15 48456643 frameshift variant A/- delins 1
rs1057519502
FBN1
1.000 0.160 15 48495237 stop gained G/A snv 1
rs1057520617
FBN1
1.000 0.160 15 48430770 missense variant A/G snv 1
rs1057520728
FBN1
1.000 0.160 15 48422057 missense variant A/C;G snv 1
rs1060501013
FBN1
1.000 0.160 15 48488410 frameshift variant C/- del 1
rs1060501014
FBN1
1.000 0.160 15 48415567 missense variant A/G snv 1
rs1060501016
FBN1
1.000 0.160 15 48428395 stop gained A/T snv 1
rs1060501019
FBN1
1.000 0.160 15 48534131 missense variant A/C snv 1
rs1060501024
FBN1
1.000 0.160 15 48503820 stop gained C/A snv 1
rs1060501026
FBN1
1.000 0.160 15 48474299 missense variant C/G snv 1
rs1060501027
FBN1
1.000 0.160 15 48503871 frameshift variant -/T ins 1
rs1060501031
FBN1
1.000 0.160 15 48463212 frameshift variant G/- del 1
rs1060501034
FBN1
1.000 0.160 15 48436986 stop gained A/T snv 1
rs1060501035
FBN1
1.000 0.160 15 48537755 stop gained G/A snv 1
rs1060501038
FBN1
1.000 0.160 15 48520672 frameshift variant G/- delins 1
rs1060501039
FBN1
1.000 0.160 15 48474554 stop gained C/T snv 1
rs1060501040
FBN1
1.000 0.160 15 48488411 stop gained A/C;T snv 1
rs1060501041
FBN1
1.000 0.160 15 48508665 missense variant C/G;T snv 1
rs1060501042
FBN1
1.000 0.160 15 48421606 frameshift variant -/T ins 1
rs1060501043
FBN1
1.000 0.160 15 48470723 frameshift variant CA/- delins 1
rs1060501044
FBN1
1.000 0.160 15 48437872 missense variant C/A snv 1
rs1060501047
FBN1
1.000 0.160 15 48600172 stop gained G/A snv 1
rs1060501048
FBN1
1.000 0.160 15 48437918 splice acceptor variant C/G;T snv 1
rs1060501050
FBN1
1.000 0.160 15 48534141 frameshift variant C/- delins 1
rs1060501051
FBN1
1.000 0.160 15 48428380 frameshift variant C/- delins 1