Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9833888 1.000 0.080 3 100004736 intron variant G/T snv 0.18 1
rs1190983
EVL
0.925 0.080 14 100031649 intron variant T/C snv 0.61 2
rs9837602 1.000 0.080 3 100105841 intron variant G/A snv 0.18 1
rs181337095 1.000 0.080 15 100366889 intergenic variant G/A snv 1
rs2273802 0.925 0.080 14 100376562 5 prime UTR variant G/A snv 0.33 2
rs612683 1.000 0.080 1 100414772 intron variant A/T snv 0.38 1
rs11292 0.925 0.080 10 100553850 3 prime UTR variant A/G snv 0.22 2
rs17094222 0.925 0.080 10 100635683 intergenic variant T/C snv 0.17 3
rs10165970 0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs17024869 0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs747097215 1.000 0.080 7 100856990 missense variant C/T snv 2.0E-05 2.1E-05 1
rs17024926 0.851 0.120 2 100889540 intron variant T/C snv 0.34 4
rs895520 0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs7581886 0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs2305160 0.776 0.200 2 100974842 missense variant A/G snv 0.71 0.75 9
rs4919510 0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs11541353 0.851 0.120 2 100977729 missense variant C/T snv 0.14 0.14 4
rs3739008 0.925 0.080 2 100996106 3 prime UTR variant C/T snv 0.24 2
rs500760
PGR
0.882 0.120 11 101039260 synonymous variant T/C snv 0.24 0.29 3
rs10895054
PGR
0.925 0.080 11 101039579 intron variant A/T snv 0.11 2
rs575018 1.000 0.080 5 101043689 intergenic variant C/G;T snv 1
rs1042839
PGR
0.925 0.080 11 101051471 synonymous variant G/A snv 0.13 0.11 2
rs56103835 0.925 0.080 14 101056219 non coding transcript exon variant T/A;C snv 4.0E-06; 0.28 2
rs1042838
PGR
0.742 0.240 11 101062681 missense variant C/A;G snv 0.13; 4.0E-06 12
rs590688
PGR
0.925 0.080 11 101105243 intron variant C/G snv 0.47 2