Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1805007 0.695 0.280 16 89919709 missense variant C/A;G;T snv 4.4E-02 25
rs1805008 0.732 0.240 16 89919736 missense variant C/T snv 4.7E-02 4.8E-02 16
rs885479 0.732 0.280 16 89919746 missense variant G/A snv 0.15 8.3E-02 16
rs2228479 0.763 0.280 16 89919532 missense variant G/A;C snv 7.8E-02; 4.0E-06 11
rs1805009 0.790 0.280 16 89920138 missense variant G/A;C snv 4.0E-06; 9.1E-03 9
rs1805005 0.827 0.080 16 89919436 missense variant G/T snv 8.6E-02 8.0E-02 8
rs1805006 0.790 0.080 16 89919510 missense variant C/A;G snv 5.2E-03; 4.0E-06 8
rs1110400 1.000 0.040 16 89919722 missense variant T/C snv 5.6E-03 6.6E-03 3
rs34090186 0.882 0.080 16 89919458 missense variant G/A snv 9.6E-04 2.7E-04 3
rs11547464 1.000 0.040 16 89919683 missense variant G/A snv 5.3E-03 4.7E-03 2
rs1232525952 0.925 0.080 16 89919597 synonymous variant G/A snv 8.1E-06 2
rs1340863788 0.925 0.080 16 89919595 missense variant C/A;T snv 2
rs371055548 0.925 0.080 16 89919798 synonymous variant C/T snv 2.4E-05 2.1E-05 2
rs201326893 1.000 0.040 16 89919714 stop gained C/A snv 8.4E-04 5.4E-04 1
rs374827260 1.000 0.040 16 89919608 missense variant A/G;T snv 4.1E-06; 1.2E-05 1