Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs4652 0.752 0.200 14 55138318 missense variant A/C snv 4.1E-06; 0.45 0.57 12
rs7628626 0.925 0.120 3 119525574 3 prime UTR variant A/C snv 0.82 2
rs11225395 0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs4671393 0.790 0.400 2 60493816 intron variant A/C;G snv 11
rs6510502 1.000 0.080 19 35647577 upstream gene variant A/C;G snv 2
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs2228468 0.882 0.120 3 42865620 missense variant A/C;T snv 0.43; 8.3E-03 6
rs11581557 1.000 0.080 1 39862786 intron variant A/C;T snv 1
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs11615 0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs20541 0.585 0.720 5 132660272 missense variant A/G snv 0.72 0.77 52
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs2071559
KDR
0.667 0.680 4 55126199 upstream gene variant A/G snv 0.53 26
rs3741219 0.776 0.280 11 1995389 non coding transcript exon variant A/G snv 0.42 10
rs11064 0.807 0.120 5 119393693 3 prime UTR variant A/G snv 0.27 9
rs13252298 0.827 0.160 8 127082911 non coding transcript exon variant A/G snv 0.24 8
rs1536309 0.851 0.160 10 102435445 upstream gene variant A/G snv 0.32 7
rs2236338 0.851 0.120 14 24631076 missense variant A/G snv 0.24 0.25 6
rs2105269 0.882 0.120 14 69280517 intron variant A/G snv 0.35 4
rs4705341 0.882 0.120 5 149426373 non coding transcript exon variant A/G snv 0.13 3
rs8105637 0.925 0.120 19 5566221 intron variant A/G snv 0.56 2