Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1004446 0.827 0.240 11 2148913 intron variant G/A snv 0.37 7
rs10045431 0.851 0.240 5 159387525 intron variant A/C snv 0.78 4
rs1014486 1.000 0.080 3 159973324 intron variant T/C snv 0.39 1
rs10201872 1.000 0.080 2 230242009 intron variant C/T snv 0.13 1
rs1021156 1.000 0.080 8 78663569 intron variant T/C snv 0.64 1
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs1036207 1.000 0.080 5 142119476 intron variant A/G;T snv 3
rs10411936 1.000 0.080 19 16437564 intron variant A/G snv 0.63 3
rs1044165 1.000 0.080 X 66021884 3 prime UTR variant G/A snv 9.0E-02 1
rs10466829 1.000 0.080 12 9723495 intron variant G/A snv 0.55 1
rs10488631 0.742 0.280 7 128954129 upstream gene variant T/C snv 9.0E-02 13
rs104895080 0.882 0.160 16 3254380 missense variant C/G;T snv 6.3E-04 3
rs104895094 0.851 0.320 16 3243403 missense variant T/A;C snv 8.0E-06; 5.2E-03 5
rs104895271 0.851 0.240 12 6334161 missense variant A/C;G snv 1.6E-04; 4.8E-05 6
rs10492503 1.000 0.080 13 92232844 intron variant T/A snv 0.36 1
rs10492972 1.000 0.080 1 10293054 intron variant T/C snv 0.32 1
rs1049353 0.630 0.600 6 88143916 synonymous variant C/T snv 0.21 0.20 42
rs10499194 0.752 0.400 6 137681500 intron variant C/T snv 0.24 10
rs10500264 1.000 0.080 19 33259408 intergenic variant G/A snv 0.14 2
rs10500817 1.000 0.080 11 15626589 intron variant T/C snv 0.12 1
rs1050391 1.000 0.080 6 32950080 non coding transcript exon variant A/G snv 0.93 1
rs10509540 0.925 0.160 10 88263276 upstream gene variant T/C snv 0.25 2
rs1051312 0.827 0.120 20 10306440 3 prime UTR variant T/C snv 0.20 5
rs10516487 0.752 0.360 4 101829919 missense variant G/A;T snv 0.26; 8.0E-06 11
rs10517086 0.882 0.160 4 26083889 intron variant G/A snv 0.27 4