Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1207112399 0.925 0.080 6 151842614 missense variant G/A snv 4.0E-06 7.0E-06 3
rs760503206 0.925 0.080 6 151807956 missense variant T/C snv 4.0E-06 2
rs767863538 0.925 0.080 6 151808207 missense variant C/G;T snv 5.6E-06; 5.6E-06 3
rs757200716 0.851 0.160 6 151842617 missense variant G/A snv 8.0E-06 5
rs2077647 0.732 0.320 6 151807942 synonymous variant T/A;C snv 8.1E-06; 0.46 16
rs747099645 0.882 0.120 6 152061061 missense variant C/T snv 1.6E-05 2.8E-05 3
rs761843408 0.925 0.080 6 152125285 synonymous variant A/G snv 3.4E-05 2.8E-05 2
rs200282497 0.925 0.080 6 151944239 missense variant G/C snv 3.6E-05 3.5E-05 4
rs188957694 0.882 0.080 6 151944218 missense variant G/A;C snv 4.0E-05 4.9E-05 6
rs201145204 0.925 0.080 6 151808318 missense variant C/T snv 2.4E-04 1.0E-03 2
rs139960913 1.000 0.080 6 151807928 missense variant C/T snv 3.3E-03 3.1E-03 1
rs200075329 0.925 0.080 6 151808264 missense variant T/C snv 4.4E-03 4.3E-03 4
rs746432 0.851 0.120 6 151808173 synonymous variant G/A;C snv 6.6E-02 7.0E-02 4
rs2273206 0.851 0.280 6 152061176 intron variant G/T snv 0.17 0.22 5
rs2228480 0.724 0.360 6 152098960 synonymous variant G/A snv 0.19 0.18 16
rs1801132 0.689 0.320 6 151944387 synonymous variant G/C snv 0.73 0.80 22