Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199473197 1.000 3 38576780 missense variant G/A;C;T snv 2.5E-05 1
rs199473335 1.000 3 38550411 missense variant G/T snv 8.8E-06 3.5E-05 1
rs199473115 1.000 3 38604837 missense variant G/A;C snv 1.2E-05; 8.0E-06 1
rs199473635 1.000 3 38550896 missense variant G/A snv 1.6E-05 1.4E-05 1
rs199473111 1.000 3 38606007 stop gained C/A;T snv 4.8E-05 6.3E-05 1
rs199473060 1.000 3 38622468 missense variant C/T snv 4.1E-06 7.0E-06 1
rs199473579 1.000 3 38598978 stop gained C/A;T snv 4.0E-06 7.0E-06 1
rs199473190 1.000 0.040 3 38579474 missense variant C/G;T snv 8.2E-06 1
rs199473627 1.000 0.040 3 38551258 missense variant A/G snv 1
rs727504495 1.000 0.080 3 38550998 missense variant C/A;T snv 4.0E-06; 2.0E-05 1
rs28937319 1.000 0.080 3 38562485 missense variant G/A snv 7.0E-06 1
rs199473118 1.000 0.080 3 38604067 missense variant G/A snv 4.4E-06 1
rs199473112 0.925 0.080 3 38605956 missense variant G/A;C snv 4.1E-06; 5.3E-05 1
rs199473621 1.000 0.080 3 38554344 missense variant C/T snv 2.0E-05 2.1E-05 1
rs199473597 1.000 0.080 3 38575307 missense variant C/T snv 1
rs199473554 0.925 0.080 3 38630392 missense variant C/T snv 1
rs199473620 1.000 0.080 3 38554372 stop gained C/A;T snv 1
rs199473302 1.000 0.080 3 38551190 missense variant A/G snv 1
rs199473228 1.000 0.080 3 38560362 missense variant A/G snv 1
rs199473206 1.000 0.080 3 38566554 missense variant C/T snv 2.4E-05 3.5E-05 1
rs199473158 1.000 0.080 3 38587519 missense variant G/A;T snv 1
rs199473092 0.925 0.080 3 38608175 missense variant A/C snv 1
rs199473299 1.000 0.080 3 38551208 missense variant T/C snv 1
rs199473205 1.000 0.080 3 38566567 missense variant A/G snv 4.0E-06 1
rs199473090 1.000 0.080 3 38608194 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 4.8E-05 1