Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs174536 11 61784455 non coding transcript exon variant A/C snv 0.29 3
rs174574 1.000 0.080 11 61832870 intron variant A/C snv 0.55 7
rs7394871 11 61885042 intron variant A/C;T snv 2
rs1000778 1.000 0.040 11 61887833 intron variant A/G snv 0.59 3
rs1260333 0.882 0.160 2 27525757 downstream gene variant A/G snv 0.58 12
rs1535 0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs174464 11 61890454 intron variant A/G snv 0.59 2
rs174472 11 61904484 intron variant A/G snv 0.41 2
rs174534 1.000 0.080 11 61781986 non coding transcript exon variant A/G snv 0.28 3
rs2072114 1.000 0.080 11 61837743 intron variant A/G snv 0.19 0.16 4
rs2727266 11 61936862 upstream gene variant A/G snv 9.8E-02 2
rs2845573 1.000 0.040 11 61834436 intron variant A/G snv 9.7E-02 3
rs2851682 11 61848540 intron variant A/G snv 9.9E-02 5
rs509360 11 61781087 intron variant A/G snv 0.61 0.52 3
rs7200543 16 15036113 synonymous variant A/G snv 0.35 0.30 6
rs17156426 11 61841851 intron variant A/G;T snv 2
rs4453795 3 192376186 intron variant A/G;T snv 2
rs10517480 4 59883111 intergenic variant A/T snv 0.27 2
rs2524299 11 61837310 intron variant A/T snv 0.17 2
rs2727271 11 61835886 intron variant A/T snv 0.12 2
rs1109748 11 61955173 synonymous variant C/A snv 0.21 0.11 2
rs174456 11 61888710 intron variant C/A snv 0.59 2
rs174476 11 61906646 synonymous variant C/A;G;T snv 0.30 2
rs174479 11 61911282 intron variant C/G snv 0.17 2
rs174575 1.000 0.040 11 61834531 intron variant C/G snv 0.25 3