Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs67507747
COL1A1
0.827 0.160 17 50194032 missense variant C/A;G;T snv 2
rs67682641
COL1A1
0.807 0.240 17 50194375 missense variant C/A;T snv 2
rs67693970
COL1A1
0.882 0.120 17 50190099 missense variant C/G;T snv 1
rs72645321
COL1A1
0.925 0.120 17 50197045 missense variant C/T snv 1
rs72645323
COL1A1
0.925 0.120 17 50197027 missense variant C/T snv 1
rs72645324
COL1A1
1.000 0.120 17 50197026 missense variant C/A snv 1
rs72645325
COL1A1
1.000 0.120 17 50197017 missense variant C/T snv 1
rs72645331
COL1A1
1.000 0.120 17 50196661 missense variant C/A snv 1
rs72645340
COL1A1
1.000 0.120 17 50196528 missense variant C/T snv 1
rs72645341
COL1A1
1.000 0.120 17 50196525 stop gained C/A;T snv 2.0E-05 1.4E-05 1
rs72645347
COL1A1
0.790 0.280 17 50196337 missense variant G/A snv 1
rs72645353
COL1A1
1.000 0.120 17 50196198 missense variant C/A;T snv 1
rs72645357
COL1A1
0.776 0.240 17 50196163 missense variant C/T snv 1
rs72645362
COL1A1
1.000 0.120 17 50195934 missense variant C/A;T snv 2.4E-05 1
rs72645365
COL1A1
0.925 0.120 17 50195656 missense variant C/A snv 1
rs72648359
COL1A1
1.000 0.120 17 50194134 missense variant G/C snv 1
rs72651627
COL1A1
1.000 0.120 17 50192519 missense variant C/T snv 1
rs72651647
COL1A1
0.925 0.120 17 50191454 missense variant C/T snv 1
rs72651658
COL1A1
0.827 0.200 17 50190861 missense variant C/T snv 7.0E-06 1
rs72653170
COL1A1
0.752 0.240 17 50188908 missense variant G/A snv 8.0E-06 1
rs72654802
COL1A1
0.882 0.120 17 50188122 missense variant C/T snv 1
rs72656323
COL1A1
1.000 0.120 17 50187076 missense variant C/T snv 1
rs72656334
COL1A1
1.000 0.120 17 50186871 missense variant C/A snv 1
rs72656339
COL1A1
1.000 0.120 17 50186797 missense variant A/C snv 1
rs72656343
COL1A1
0.882 0.120 17 50186386 stop gained C/A;T snv 1