Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10667251 0.925 0.080 17 49388381 intron variant -/TCT delins 0.47 4
rs11071559 0.925 0.080 15 60777789 intron variant C/T snv 0.23 4
rs12123821 0.925 0.080 1 152206676 intron variant C/T snv 2.9E-02 4
rs12722502 0.882 0.080 10 6051176 intron variant C/T snv 7.8E-03 4
rs143326447 0.925 0.080 2 111511155 intron variant T/C snv 0.11 4
rs17294280 0.882 0.120 15 67175947 intron variant A/G snv 0.19 4
rs2395185 0.724 0.360 6 32465390 intron variant G/T snv 0.29 4
rs3024971 0.827 0.200 12 57099944 intron variant T/G snv 7.8E-02 7.9E-02 4
rs3122929 0.882 0.080 12 57115319 intron variant C/T snv 0.33 4
rs4574025 0.882 0.160 18 62342581 intron variant C/T snv 0.55 4
rs61894547 0.882 0.160 11 76537586 intron variant C/T snv 3.1E-02 4
rs72823641 0.882 0.080 2 102319699 intron variant T/A;C snv 4
rs8005161 0.882 0.120 14 88006251 intron variant C/T snv 0.18 4
rs8034191 0.695 0.440 15 78513681 intron variant T/C snv 0.27 4
rs9272346 0.790 0.320 6 32636595 intron variant G/A snv 0.54 4
rs10519067 0.925 0.120 15 60776148 intron variant G/A snv 0.20 3
rs10791824 0.882 0.160 11 65791795 intron variant A/G;T snv 3
rs10905284 0.882 0.200 10 8073399 intron variant C/A;T snv 3
rs10995245 0.882 0.160 10 62631615 intron variant G/A;C snv 3
rs115288876 0.925 0.120 1 152027641 intron variant G/A snv 2.5E-02 3
rs117137535 0.882 0.120 9 137605991 intron variant G/A snv 2.7E-02 3
rs11715524 0.925 0.080 3 196035621 intron variant G/A snv 0.54 3
rs12952581 0.925 0.080 17 49370984 intron variant G/A snv 0.42 0.28 3
rs1295686 0.882 0.160 5 132660151 intron variant T/A;C snv 0.68 3
rs13003464 0.827 0.200 2 60959694 intron variant A/G snv 0.50 3