Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12953 0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 9
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs1535045 0.742 0.360 20 46119460 intron variant C/A;G;T snv 12
rs17228212 0.807 0.160 15 67166301 intron variant T/C snv 0.21 8
rs17231520 0.851 0.240 16 56961915 upstream gene variant G/A snv 2.1E-02 9
rs1800795 0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1800871 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs1800872 0.495 0.840 1 206773062 5 prime UTR variant T/G snv 0.69 119
rs1800896 0.507 0.800 1 206773552 intron variant T/C snv 0.41 113
rs1805192 0.510 0.840 3 12379739 missense variant C/G snv 121
rs1862513 0.763 0.360 19 7668907 upstream gene variant C/G;T snv 11
rs1878406 0.807 0.200 4 147472512 intergenic variant C/A;G;T snv 7
rs2167270
LEP
0.724 0.280 7 128241296 5 prime UTR variant G/A snv 0.37 17
rs3939286 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 12
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 10
rs549858786 0.790 0.320 2 112836807 5 prime UTR variant T/A snv 10
rs563558831 0.776 0.320 19 40991226 upstream gene variant T/C snv 7.0E-06 11
rs587745372 0.851 0.240 1 147773383 upstream gene variant T/A snv 2.8E-05 7
rs599839 0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs63750953
HBB
0.790 0.400 11 5227097 5 prime UTR variant TT/- delins 7.0E-06 10
rs72661131 0.742 0.480 10 52771739 upstream gene variant A/G snv 7.6E-04 15
rs7903146 0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs11556924 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 21