Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10034228 0.882 0.040 4 111690594 intergenic variant T/C snv 0.32 1
rs10113215 1.000 0.040 8 59219635 intergenic variant A/G snv 0.33 1
rs10512441 1.000 0.040 17 32912627 regulatory region variant C/T snv 0.21 1
rs11658305 1.000 0.040 17 7526004 intergenic variant A/C;T snv 1
rs1370156 1.000 0.040 15 34692682 intergenic variant G/C snv 0.67 1
rs1556867 1.000 0.040 1 164244449 intergenic variant C/T snv 0.24 1
rs4373767 0.882 0.040 1 219586340 regulatory region variant C/T snv 0.32 1
rs61049169 1.000 0.040 2 146131140 intergenic variant G/A;C snv 1
rs73157695 1.000 0.040 21 45952033 intergenic variant G/A snv 0.29 1
rs9585327 1.000 0.040 13 100037100 intergenic variant G/A snv 0.36 1
rs8027411 0.882 0.040 15 79168687 intron variant G/T snv 0.52 1
rs7162310 1.000 0.040 15 63279035 intron variant C/T snv 0.28 1
rs4948523 1.000 0.040 10 58579338 intron variant A/C snv 0.51 1
rs5022942 1.000 0.040 4 81038812 intron variant A/G snv 0.59 1
rs5442 0.925 0.120 12 6845700 missense variant G/A snv 4.8E-02 4.6E-02 1
rs34016308 1.000 0.040 14 92149397 intron variant -/TA delins 0.19 1
rs397515624 0.851 0.040 21 43169133 missense variant C/T snv 4.0E-06 1
rs2155413 1.000 0.040 11 84923746 intron variant C/A snv 0.55 1
rs10892173 1.000 0.040 11 117801846 3 prime UTR variant C/T snv 0.38 1
rs201140091 1.000 0.040 10 48200198 intron variant A/-;AAAAA;AAAAAA;AAAAAAAAA;AAAAAAAAAA;AAAAAAAAAAA;AAAAAAAAAAAAA;AAAAAAAAAAAAAA delins 1
rs297589 1.000 0.040 2 156502238 intron variant T/A snv 0.65 1
rs71041628 1.000 0.040 11 105794433 intron variant GTGTGTGTGT/-;GTGT;GTGTGT;GTGTGTGT;GTGTGTGTGTGT delins 0.67 1
rs10824518 0.882 0.040 10 77303784 intron variant T/A;C snv 1
rs2808510 1.000 0.040 1 200366947 non coding transcript exon variant C/T snv 0.29 1
rs2342406 1.000 0.040 2 44925609 intron variant T/C snv 0.19 1