Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs5186 0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs2514259
AIP
0.807 0.280 11 67479201 upstream gene variant C/G;T snv 8
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1800497 0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs3135506 0.708 0.400 11 116791691 missense variant G/A;C snv 3.0E-05; 6.8E-02 26
rs662799 0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs2781666 0.790 0.280 6 131572419 intron variant G/T snv 0.45 8
rs1800469 0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs6929846 0.827 0.160 6 26458037 5 prime UTR variant T/C snv 0.70 10
rs1001179
CAT
0.641 0.680 11 34438684 upstream gene variant C/T snv 0.16 33
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs5443 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs7756992 0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs1333045 0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs1333049 0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs2383206 0.742 0.320 9 22115027 intron variant A/G snv 0.49 17
rs2383207 0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs4977574 0.695 0.520 9 22098575 intron variant A/G;T snv 26
rs1800775 0.790 0.240 16 56961324 upstream gene variant C/A;G snv 0.51; 5.7E-06 18