Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143383
GDF5
0.724 0.320 20 35438203 5 prime UTR variant G/A snv 0.47 17
rs143384
GDF5
0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 17
rs224333
GDF5
20 35436182 intron variant A/G snv 0.47 3
rs121909349
GDF5-AS1 ; GDF5
0.882 0.040 20 35434297 missense variant A/C snv 3
rs74315388
GDF5-AS1 ; GDF5
0.882 0.080 20 35434102 missense variant C/A;T snv 3
rs28936683
GDF5 ; GDF5-AS1
0.882 0.080 20 35434093 missense variant A/G snv 7.0E-06 3
rs224334
GDF5
20 35436939 intron variant A/G snv 0.92 2
rs739329
GDF5
20 35439830 intron variant G/A snv 3.0E-02 2
rs224330
GDF5-AS1 ; GDF5
20 35434398 synonymous variant T/C snv 0.90 2
rs224332
GDF5-AS1 ; GDF5
20 35434874 missense variant A/C;G snv 2
rs397514519
GDF5 ; GDF5-AS1
0.925 0.080 20 35434220 missense variant G/A snv 4.0E-06 2
rs74315389
GDF5 ; GDF5-AS1
0.925 0.080 20 35433944 missense variant C/T snv 8.0E-06 1.4E-05 2
rs28936397
GDF5
1.000 0.080 20 35437412 missense variant T/C;G snv 8.0E-06; 4.0E-06 1
rs6120946
GDF5
20 35442075 intron variant A/T snv 0.21 1
rs121909348
GDF5-AS1 ; GDF5
1.000 0.080 20 35433954 stop gained A/C snv 1
rs1568731526
GDF5-AS1 ; GDF5
1.000 0.080 20 35434271 frameshift variant C/- delins 1
rs368375586
GDF5-AS1 ; GDF5
1.000 0.080 20 35434459 missense variant C/A;T snv 6.1E-05 1
rs397514668
GDF5-AS1 ; GDF5
1.000 0.080 20 35434276 missense variant C/T snv 4.0E-06 1
rs74315386
GDF5-AS1 ; GDF5
1.000 0.080 20 35434514 stop gained G/A snv 1
rs886039878
GDF5-AS1 ; GDF5
1.000 0.080 20 35434018 missense variant C/T snv 1
rs121909347
GDF5 ; GDF5-AS1
1.000 0.080 20 35433991 missense variant C/T snv 1
rs121909350
GDF5 ; GDF5-AS1
1.000 0.080 20 35434282 missense variant C/A;T snv 4.0E-06; 4.0E-06 1
rs121909351
GDF5 ; GDF5-AS1
1.000 0.080 20 35434109 missense variant G/T snv 1
rs74315387
GDF5 ; GDF5-AS1
1.000 0.080 20 35434216 stop gained C/T snv 1