Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10757272 0.851 0.160 9 22088261 intron variant C/T snv 0.41 6
rs10757274 0.701 0.320 9 22096056 intron variant A/G snv 0.41 22
rs10757277 1.000 0.040 9 22124451 intron variant A/G snv 0.40 2
rs10757278 0.620 0.520 9 22124478 intron variant A/G snv 0.40 44
rs10757279 0.925 0.040 9 22124631 intron variant A/G snv 0.40 3
rs10807323 6 12794799 intron variant G/A snv 0.34 1
rs10811641 1.000 0.040 9 22014138 non coding transcript exon variant C/G snv 0.32 2
rs10811643 1.000 0.040 9 22024967 intron variant A/G snv 0.56 2
rs10811645 1.000 0.040 9 22049657 intron variant G/A snv 0.59 2
rs10811647 1.000 0.040 9 22065003 intron variant C/G;T snv 3
rs10811650 0.882 0.200 9 22067594 intron variant A/G snv 0.37 5
rs10811651 1.000 0.040 9 22067831 intron variant G/A;C snv 2
rs10811656 0.807 0.200 9 22124473 intron variant C/T snv 0.47 7
rs10889332 1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39 4
rs10965212 0.925 0.080 9 22023796 intron variant T/A;C;G snv 3
rs10965215 0.882 0.120 9 22029446 missense variant G/A snv 0.55 0.46 4
rs10965219 0.882 0.080 9 22053688 intron variant A/G snv 0.58 4
rs10965224 1.000 0.040 9 22067277 intron variant T/A snv 0.64 2
rs10978777 1.000 0.080 9 107268309 intergenic variant G/A;C snv 2
rs113533135 1.000 0.080 2 140268867 intron variant T/C snv 2.0E-02 2
rs113805659 1.000 0.080 7 78663475 intron variant G/C snv 6.1E-02 2
rs114031744 1.000 0.080 10 123610085 intergenic variant A/G snv 1.7E-02 2
rs11509197 1.000 0.080 7 118641356 intergenic variant C/T snv 0.38 2
rs115689251 1.000 0.080 17 36032377 intergenic variant A/C snv 1.0E-02 2
rs117854110 1.000 0.080 7 105603002 upstream gene variant C/A;T snv 2