Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12598357 0.724 0.240 16 28329624 intergenic variant A/G snv 0.43 15
rs7302200 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 6
rs2388334 0.882 0.040 6 98143746 intron variant A/G snv 0.39 5
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs6012558 20 48914749 intergenic variant G/A snv 0.42 4
rs6774721 1.000 0.040 3 49344465 upstream gene variant G/A snv 0.15 4
rs6855246 1.000 0.040 4 102191313 intergenic variant A/G snv 0.14 4
rs10149470 1.000 0.040 14 103551616 upstream gene variant A/G snv 0.54 3
rs10774547 0.925 0.120 12 120424913 intergenic variant T/C snv 0.39 3
rs1541374 4 105127203 intergenic variant T/A;G snv 3
rs2008514 16 28814284 non coding transcript exon variant G/A snv 0.35 3
rs28600726 1.000 0.040 4 158730723 intergenic variant G/A snv 0.53 3
rs3843954 1.000 0.040 13 57974377 intergenic variant G/A;C snv 3
rs475616 10 30207976 regulatory region variant A/G snv 0.67 3
rs55771711 1.000 0.040 10 131989233 intergenic variant G/C snv 0.24 3
rs61572747 1.000 0.040 17 45383525 regulatory region variant A/G snv 0.25 3
rs6940116 1.000 0.040 6 27740953 upstream gene variant A/G snv 0.18 3
rs7613360 1.000 0.040 3 49879277 upstream gene variant C/T snv 0.32 3
rs901630 6 98091643 intron variant C/T snv 0.32 3
rs1008078 1.000 0.040 1 90724174 non coding transcript exon variant C/T snv 0.33 2
rs10129426 14 103552118 upstream gene variant G/A snv 0.54 2
rs10192369 2 160524377 intergenic variant G/A snv 0.45 2
rs10757417 1.000 0.040 9 23347855 intron variant G/A;T snv 2
rs1076884 1.000 0.040 16 13653946 intergenic variant C/G;T snv 2
rs10791106 1.000 0.040 11 130976537 intergenic variant A/G snv 0.45 2