Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1413711 0.882 0.200 6 43772941 intron variant T/A;C snv 3
rs1222213359 0.574 0.720 6 43770966 missense variant G/A snv 62
rs1287276985 0.790 0.200 6 43782020 missense variant T/A;C snv 4.0E-06; 4.0E-06 7.0E-06 7
rs1443465532 0.882 0.080 6 43774362 missense variant G/C snv 4.0E-06 7.0E-06 6
rs752907384 0.827 0.200 6 43782077 missense variant C/G;T snv 8.0E-06 6
rs1188254133 0.851 0.240 6 43781990 missense variant T/G snv 7.0E-06 4
rs1284410244 0.925 0.040 6 43778482 missense variant A/G snv 7.0E-06 4
rs138551969 1.000 0.040 6 43780749 missense variant A/G snv 1.2E-05 3.5E-05 4
rs914956206 0.882 0.080 6 43770762 missense variant G/A;T snv 4
rs374057152 0.925 0.200 6 43777592 missense variant T/C snv 4.0E-06 1.4E-05 3
rs752153816 0.882 0.120 6 43780848 missense variant G/A;C snv 4.0E-06; 4.0E-06; 1.2E-05; 3.6E-05 3
rs1212415280 6 43771130 missense variant G/T snv 2.1E-05 2
rs1243046808 0.925 0.160 6 43770758 missense variant C/G;T snv 2.0E-05; 9.8E-06 2
rs1365501228 1.000 0.080 6 43770732 missense variant C/T snv 1.4E-05 2
rs140461341 6 43782078 missense variant G/A snv 3.6E-05 4.2E-05 2
rs748352475 0.925 0.160 6 43777546 missense variant C/G snv 1.2E-05 7.0E-06 2
rs766474822 0.925 0.080 6 43770990 missense variant G/A snv 1.4E-05 2.1E-05 2
rs771561387 1.000 0.080 6 43784557 missense variant C/G;T snv 4.0E-06; 1.2E-05 2
rs1201894677 6 43770833 missense variant G/A snv 1.6E-05 1
rs1229919945 1.000 0.040 6 43782041 missense variant T/C snv 1
rs1346131223 1.000 6 43777657 missense variant A/G snv 7.4E-06 1
rs1404013760 1.000 0.040 6 43771137 missense variant G/C snv 8.9E-06 1
rs141138308 1.000 0.040 6 43780784 missense variant C/A;T snv 4.0E-06; 2.8E-05 1
rs1421145908 6 43777618 missense variant G/A snv 7.0E-06 1
rs376388064 6 43782006 missense variant C/T snv 2.8E-05 3.5E-05 1