Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs10735810
VDR
0.662 0.640 12 47879112 start lost A/C;G;T snv 26
rs11833579 0.827 0.200 12 666033 upstream gene variant G/A snv 0.25 6
rs17000900
MX1
0.925 0.120 21 41426103 5 prime UTR variant C/A snv 0.14 2
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1800587 0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
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
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
rs397507444 0.405 0.880 1 11794407 missense variant T/G snv 306
rs4950928 0.653 0.560 1 203186754 upstream gene variant G/A;C;T snv 33
rs57095329 0.677 0.480 5 160467840 intron variant A/G snv 7.8E-02 25
rs699947 0.570 0.680 6 43768652 upstream gene variant A/C;T snv 67
rs7120118 0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs8702 0.851 0.160 14 103686015 3 prime UTR variant C/G snv 0.61 5
rs9268877 0.827 0.200 6 32463370 intron variant A/G;T snv 5
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs746682028 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs4986790 0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs2910164 0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs61752717 0.583 0.840 16 3243407 missense variant T/A;C snv 2.8E-04 72
rs1800562 0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262