Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2042555 1.000 0.040 2 147797920 intergenic variant G/A snv 0.34 2
rs2090408 1.000 0.040 3 107479604 intergenic variant G/T snv 0.32 2
rs2149351 1.000 0.040 9 117739366 intron variant T/G snv 0.81 2
rs2396133 1.000 0.040 7 109557010 intron variant A/G snv 0.47 2
rs2688708 1.000 0.040 11 55073194 intergenic variant C/G;T snv 2
rs34807503 1.000 0.040 12 51525350 intergenic variant ATTTATTT/-;ATTT;ATTTATTTATTT delins 2
rs35738585 1.000 0.040 11 113515625 intergenic variant T/G snv 0.40 2
rs4257287 1.000 0.040 18 55076600 intergenic variant C/T snv 0.87 2
rs4373974 1.000 0.040 11 113559764 intergenic variant T/G snv 0.40 2
rs4578918 1.000 0.040 20 46093017 upstream gene variant T/C snv 0.77 2
rs56403421 1.000 0.040 18 55098052 regulatory region variant A/C snv 0.26 2
rs57506017 1.000 0.040 7 12205599 intergenic variant A/T snv 0.28 2
rs6130328 1.000 0.040 20 43256482 intergenic variant G/A snv 0.54 2
rs61687445 1.000 0.040 11 113567370 intergenic variant C/A snv 0.35 2
rs62199592 2 183858773 intergenic variant A/G snv 2.1E-02 2
rs6779928 1.000 0.040 3 16717777 intergenic variant G/A;C snv 2
rs6795372 1.000 0.040 3 136765048 intergenic variant T/G snv 0.42 2
rs76923064 1.000 0.040 2 156300636 downstream gene variant T/C snv 1.2E-02 2
rs77607745 1.000 0.040 13 69001052 intergenic variant A/C snv 0.15 2
rs7827176 1.000 0.040 8 91637324 intron variant A/T snv 0.55 2
rs7912226 1.000 0.040 10 105892386 intron variant T/A snv 0.44 2
rs7927693 1.000 0.040 11 113554746 intergenic variant G/A snv 0.57 2
rs7937477 1.000 0.040 11 113545374 intergenic variant A/T snv 0.59 2
rs836927 1.000 0.040 3 107482581 intergenic variant C/A snv 0.52 2
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 2