Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11597086 10 100193948 non coding transcript exon variant A/C snv 0.30 0.29 1
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
rs12097137 1 101243889 downstream gene variant G/A;T snv 3
rs12101753 15 101446855 intron variant T/C snv 4.3E-02 1
rs28385681 2 102017062 intron variant T/G snv 1.4E-05 1
rs3917237 2 102155991 intron variant G/A snv 1.9E-02 1
rs13107325 0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 8
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
rs7938449 11 102778167 intron variant C/A;T snv 1
rs11760826 7 103151364 upstream gene variant A/C;G snv 1
rs1997243 7 1044141 intron variant A/G snv 0.11 1
rs9282541 0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 2
rs4149273 9 104879930 intron variant T/C snv 0.45 3
rs4149272 9 104880006 intron variant C/G;T snv 0.48 3
rs11789603 9 104884738 intron variant C/T snv 0.11 2
rs4149269 9 104884840 intron variant A/G snv 0.41 3
rs4149268 1.000 0.040 9 104884939 intron variant C/T snv 0.46 4
rs3890182 0.925 0.120 9 104885374 intron variant G/A;T snv 4
rs3847300 9 104886149 intron variant G/A snv 0.12 3
rs13290420 9 104886684 intron variant T/C snv 0.16 3