Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs311686 1.000 0.040 6 73416152 missense variant A/G snv 0.52 0.48 1
rs751273816 1.000 0.040 1 47373057 missense variant G/A snv 4.0E-06 1
rs12294076 1.000 0.040 11 103256336 intron variant T/C snv 6.8E-02 1
rs7675690 1.000 0.040 4 74382934 intron variant A/G snv 9.3E-02 1
rs1045481 1.000 0.040 17 744917 missense variant G/A;C snv 0.20 1
rs865901367 1.000 0.040 22 39968124 missense variant C/T snv 2.1E-05 1
rs534448891 1.000 0.040 16 85413567 intron variant C/G;T snv 6.3E-05 1
rs41553512 1.000 0.040 6 32518625 missense variant C/T snv 0.12 4.6E-02 1
rs10507172 1.000 0.040 12 103949490 intron variant G/A snv 7.2E-02 1
rs10507173 1.000 0.040 12 103950058 intron variant A/G snv 6.3E-02 1
rs1190662183 1.000 0.040 19 10338932 synonymous variant C/T snv 1
rs1101998 1.000 0.040 1 159029494 intron variant C/T snv 0.65 1
rs1633256 1.000 0.040 1 159032767 intron variant A/G snv 0.70 1
rs41401746 1.000 0.040 6 137219797 upstream gene variant AA/- del 2.0E-02 1
rs56251346 1.000 0.040 6 137199749 intron variant C/T snv 0.20 1
rs9376269 1.000 0.040 6 137218368 intron variant C/G snv 0.22 1
rs5744247 1.000 0.040 11 112155433 intron variant G/C snv 8.9E-02 1
rs3218255 1.000 0.040 22 37148446 intron variant G/A snv 0.21 1
rs11567764 1.000 0.040 5 35873503 missense variant G/A;T snv 9.5E-03; 4.0E-06 1
rs11246213 1.000 0.040 11 612967 intron variant A/G snv 0.25 0.33 1
rs10051924 1.000 0.040 5 150847077 5 prime UTR variant T/C snv 0.21 1
rs12654043 1.000 0.040 5 150846533 5 prime UTR variant A/C;G snv 1
rs11958933 1.000 0.040 5 25323598 intron variant G/A snv 0.70 1
rs931924 1.000 0.040 5 25321925 intron variant C/T snv 0.70 1
rs3212220 1.000 0.040 5 159327187 intron variant C/A snv 0.26 1