Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72656349
COL1A1
1.000 0.120 17 50185789 missense variant C/T snv 1
rs72656348
COL1A1
1.000 0.120 17 50185863 missense variant A/C snv 1
rs72656343
COL1A1
0.882 0.120 17 50186386 stop gained C/A;T snv 3
rs72656342
COL1A1
1.000 0.120 17 50186493 missense variant C/G snv 1
rs66948146
COL1A1
1.000 0.120 17 50186894 missense variant C/A snv 1
rs72656332
COL1A1
0.882 0.120 17 50186895 missense variant C/T snv 3
rs72656331
COL1A1
0.925 0.120 17 50186903 missense variant C/A snv 2
rs72656330
COL1A1
0.925 0.120 17 50186913 missense variant C/T snv 2
rs72656325
COL1A1
1.000 0.120 17 50187031 missense variant C/T snv 1
rs72656324
COL1A1
0.925 0.120 17 50187050 missense variant C/A snv 2
rs72656322
COL1A1
1.000 0.120 17 50187086 missense variant C/G snv 1
rs72656321
COL1A1
0.925 0.120 17 50187094 missense variant C/A;T snv 2
rs72656317
COL1A1
1.000 0.120 17 50187122 missense variant C/T snv 1
rs72656312
COL1A1
1.000 0.120 17 50187537 missense variant C/A snv 1
rs72656311
COL1A1
1.000 0.120 17 50187928 missense variant C/G snv 1
rs72656308
COL1A1
1.000 0.120 17 50187946 missense variant C/T snv 1
rs72656305
COL1A1
1.000 0.120 17 50187982 missense variant C/G snv 1
rs72654802
COL1A1
0.882 0.120 17 50188122 missense variant C/T snv 3
rs72653178
COL1A1
0.925 0.120 17 50188619 missense variant C/T snv 2
rs72653172
COL1A1
0.925 0.120 17 50188768 missense variant C/T snv 2
rs67771061
COL1A1
0.925 0.120 17 50188776 missense variant C/A;G;T snv 2
rs72653167
COL1A1
1.000 0.120 17 50188947 missense variant C/A snv 1
rs72653166
COL1A1
0.925 0.120 17 50189009 missense variant C/A snv 2
rs72653159
COL1A1
1.000 0.120 17 50189266 missense variant C/A snv 1
rs72653154
COL1A1
0.925 0.120 17 50189430 missense variant C/A snv 2