Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17883880 10 100230590 intron variant T/A snv 1.2E-02 4
rs11224571
PGR
11 101047942 intron variant C/A snv 1.2E-02 3
rs7928851
PGR
11 101117160 intron variant C/A snv 1.7E-02 3
rs11571151 11 101127486 missense variant C/G;T snv 6
rs7952037 11 102379653 downstream gene variant C/T snv 1.9E-02 3
rs5030339 19 10269461 intron variant G/A snv 3.4E-03 5
rs5030359 19 10277786 intron variant G/A snv 2.1E-03 3
rs13465 19 10692116 3 prime UTR variant A/C;G snv 3
rs585362 1 109247173 upstream gene variant C/G;T snv 4
rs10858082 1 109256099 intron variant G/A snv 0.48 3
rs4970833 1 109262024 intron variant G/A snv 0.36 3
rs6698843 0.925 0.080 1 109264212 synonymous variant C/A;T snv 4.0E-06; 0.44 3
rs6689614 1 109264477 synonymous variant G/A;C snv 0.44 3
rs6657811 1 109264661 intron variant A/C;T snv 4.0E-06; 0.10 3
rs17035665 1 109271097 intron variant C/T snv 0.19 3
rs4970834 0.925 0.160 1 109272258 intron variant C/T snv 0.17 0.21 6
rs611917 1.000 0.040 1 109272630 non coding transcript exon variant A/G snv 0.28 0.32 4
rs7528419 0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 7
rs12740374 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 8
rs660240 1 109275216 3 prime UTR variant T/C snv 0.75 5
rs3832016 1 109275536 3 prime UTR variant -/T ins 0.74 3
rs57677983 1 109275536 3 prime UTR variant C/A;G;T snv 1.1E-02 3
rs629301 0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 8
rs646776 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 10
rs55882046 1 109277359 downstream gene variant C/T snv 6.7E-02 3