Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1442808 1.000 0.080 15 98221618 intron variant T/A;C snv 1
rs149096812 1.000 0.080 5 111082543 intron variant T/C snv 1.1E-02 1
rs1491921 1.000 0.080 5 21259029 intergenic variant G/T snv 0.95 1
rs150260796 1.000 0.080 17 40012575 non coding transcript exon variant A/C;G snv 1
rs1538084 1.000 0.080 1 152523536 intergenic variant A/C snv 0.79 1
rs16929496 1.000 0.080 12 25840870 regulatory region variant T/C snv 0.19 1
rs17406680 1.000 0.080 10 9166241 regulatory region variant G/C snv 3.2E-02 1
rs17572584 1.000 0.080 3 143169201 intergenic variant C/T snv 0.11 1
rs17637472 1.000 0.080 17 49384071 intron variant G/A snv 0.28 1
rs17642749 1.000 0.080 10 117887745 intergenic variant T/G snv 5.6E-02 1
rs1776883 1.000 0.080 6 34188667 upstream gene variant C/T snv 0.58 1
rs1861760 1.000 0.080 16 50823782 intergenic variant A/C;T snv 1
rs202011557 1.000 0.080 2 102297182 intergenic variant -/CAA delins 1
rs2074439 1.000 0.080 17 43615238 downstream gene variant G/C;T snv 1
rs2153101 1.000 0.080 1 203199346 intergenic variant A/T snv 0.84 1
rs2253717 1.000 0.080 17 40711984 intergenic variant G/A snv 0.26 1
rs2381413 1.000 0.080 9 6167017 intergenic variant C/G;T snv 1
rs2425656 1.000 0.080 20 44877606 intron variant G/A snv 0.32 1
rs2427829 1.000 0.080 1 159312221 downstream gene variant A/G;T snv 1
rs2431345 1.000 0.080 5 123802198 regulatory region variant T/A;C snv 1
rs2477923 1.000 0.080 10 8524027 intergenic variant T/A;C snv 1
rs2538026 1.000 0.080 18 56261410 intergenic variant A/C;G snv 1
rs2549003 1.000 0.080 5 132493605 intron variant G/A;C snv 1
rs2586731 1.000 0.080 18 50790789 downstream gene variant G/C;T snv 0.91 1
rs2675724 1.000 0.080 6 165152406 intergenic variant A/C;T snv 1