Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs261332 0.851 0.120 15 58435126 non coding transcript exon variant A/G snv 0.80 20
rs1051931 0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs1801252 0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs10224002 0.925 0.080 7 151717955 intron variant A/G snv 0.31 12
rs20455 0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs5065 0.763 0.240 1 11846011 stop lost A/G snv 0.14 0.21 12
rs1926447 0.807 0.440 13 46055809 missense variant A/G snv 0.74 0.77 11
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs1265538677 0.790 0.200 13 46055808 synonymous variant A/G snv 4.0E-06 10
rs41507953 0.790 0.280 8 27500988 missense variant A/G snv 8.7E-02 0.13 10
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs2266780 0.827 0.280 1 171114102 missense variant A/G snv 0.15 0.14 9
rs10903323 0.807 0.160 8 10292057 intron variant A/G snv 0.15 8
rs1801020 1.000 0.040 5 177409531 5 prime UTR variant A/G snv 0.65 0.67 8
rs1984112 0.807 0.280 7 80613604 intron variant A/G snv 0.33 8
rs1194897557 0.827 0.240 1 11796276 missense variant A/G snv 8.0E-06 7
rs2359612 0.851 0.120 16 31092475 intron variant A/G snv 0.66 7
rs9370867 0.827 0.120 6 16145094 missense variant A/G snv 0.60 0.63 7
rs10838738 1.000 0.080 11 47641497 intron variant A/G snv 0.28 6