Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113994095 0.701 0.360 15 89327201 missense variant C/T snv 5.1E-04 6.7E-04 21
rs8321 0.742 0.320 6 30064745 3 prime UTR variant A/C snv 5.4E-02 5.9E-02 15
rs11191580 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 12
rs174576 0.851 0.200 11 61836038 intron variant C/A;T snv 12
rs1333048 0.683 0.320 9 22125348 intron variant A/C snv 0.44 10
rs1480380 0.763 0.360 6 32945469 intron variant C/T snv 0.11 10
rs886424 0.776 0.320 6 30814225 non coding transcript exon variant C/T snv 7.1E-02 8.7E-02 10
rs5742904 0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 9
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs1006737 0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs1516725 0.925 0.120 3 186106215 intron variant T/C snv 0.86 7
rs2710323 0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs8040868 0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 7
rs9275524 0.807 0.160 6 32707332 upstream gene variant T/C snv 0.58 7
rs12576775 0.827 0.080 11 79366149 intron variant A/G snv 0.15 6
rs1333045 0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 6
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 6
rs2252865 0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs9371601 0.790 0.120 6 152469438 intron variant G/T snv 0.46 6
rs10275045 0.882 0.160 7 1881190 intron variant C/T snv 0.35 5
rs10503253 0.851 0.040 8 4323322 intron variant C/A snv 0.18 5
rs10994359 0.827 0.040 10 60462349 intron variant T/C snv 8.0E-02 5
rs10994397 0.851 0.040 10 60519366 intron variant C/T snv 9.5E-02 5
rs11152369 0.851 0.040 18 55399097 intron variant A/C snv 6.3E-02 5