Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs797046134 1.000 0.040 15 100914748 missense variant T/C snv 1
rs1553920379 0.776 0.160 4 101032294 frameshift variant -/AGTA delins 27
rs1566823361 0.742 0.440 13 101726732 frameshift variant -/G delins 18
rs34002892 0.851 0.200 12 101753470 frameshift variant GA/- delins 5.1E-04 3.5E-04 8
rs1409313 1.000 0.040 10 102431844 intron variant T/C snv 0.85 1
rs11191454 0.776 0.160 10 102900247 intron variant A/G snv 7.9E-02 5
rs11191580 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs7910584 1.000 0.040 10 106607970 intron variant C/A snv 0.65 1
rs11211996 1.000 0.040 11 106987949 intron variant T/C snv 0.15 1
rs1895729 1.000 0.040 11 107113002 intergenic variant G/A snv 0.37 1
rs10749886 1.000 0.040 11 107129809 intergenic variant G/A snv 0.35 1
rs3797817
FER
1.000 0.040 5 108948641 intron variant A/C;G snv 1
rs4773054 1.000 0.040 13 109501681 intron variant T/C snv 0.89 2
rs10498676 0.925 0.040 6 11026766 intron variant G/A snv 0.18 1
rs12877501 0.925 0.160 13 110512039 missense variant G/A;C snv 5.0E-04 4
rs6891903 1.000 0.040 5 11371193 intron variant A/G snv 6.8E-02 1
rs3782000 1.000 0.040 11 114202153 intron variant C/T snv 0.18 1
rs6537825 1.000 0.040 1 114405659 missense variant A/G snv 0.88 0.92 1
rs11582563 1.000 0.040 1 114416918 intron variant G/A snv 0.14 1
rs11585926 1.000 0.040 1 114431068 intron variant T/C snv 0.22 3
rs11589568 1.000 0.040 1 114453702 intron variant T/C snv 0.14 1
rs7511633 1.000 0.040 1 114456655 intron variant G/A snv 0.36 1
rs6661053 1.000 0.040 1 114496497 intron variant T/A;C snv 1
rs11102800 1.000 0.040 1 114498310 intron variant C/T snv 0.58 2
rs3827735 1.000 0.040 1 114510087 intron variant C/A;T snv 1