Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 28
rs1057519904 0.742 0.080 6 27872233 missense variant T/A snv 17
rs1057519902 0.742 0.160 1 226064451 missense variant G/C snv 16
rs11554137 0.742 0.040 2 208248468 synonymous variant G/A snv 5.1E-02 6.8E-02 13