Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10022462 1.000 0.080 4 88322666 intron variant C/T snv 0.41 1
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 19
rs10096351 1.000 0.080 8 127359926 intron variant A/G snv 0.60 1
rs1011970 0.677 0.320 9 22062135 intron variant G/T snv 0.23 18
rs10146997 0.827 0.240 14 79478819 intron variant A/G snv 0.25 2
rs10169133 1.000 0.080 2 19212878 intron variant G/C;T snv 0.55 1
rs1017226 0.925 0.080 5 56857565 intron variant T/C snv 5.8E-02 1
rs10235235 0.925 0.080 7 99478208 intron variant T/C snv 0.13 1
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 4
rs10269006 1.000 0.080 7 94758031 intergenic variant G/T snv 0.32 1
rs10273424 0.925 0.080 7 99598450 intron variant T/A snv 0.13 1
rs1028842 1.000 0.080 14 68205006 intron variant C/A snv 0.17 1
rs1038304 0.882 0.160 6 151612040 intron variant A/G snv 0.58 1
rs1041981 0.667 0.520 6 31573007 missense variant C/A snv 0.35 0.38 3
rs1042031 0.790 0.200 2 21002881 stop gained C/A;T snv 8.0E-06; 0.15 3
rs1045411 0.708 0.360 13 30459095 3 prime UTR variant C/T snv 0.20 2
rs10462028 0.882 0.120 4 55432133 3 prime UTR variant G/A snv 0.28 1
rs10472076 0.925 0.080 5 58888234 regulatory region variant T/A;C snv 2
rs10474352 0.925 0.080 5 91436408 intron variant C/T snv 0.23 1
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 35
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 13
rs10506868 0.716 0.160 10 112559621 intron variant C/T snv 3.1E-02 9
rs10510097 1.000 0.080 10 121568362 intron variant C/T snv 0.19 1
rs10520699 1.000 0.080 15 90979736 intron variant G/A snv 8.6E-02 1
rs1052536 0.776 0.200 17 35004556 3 prime UTR variant C/T snv 0.42 0.36 1