Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs63750874 1.000 0.160 16 16150144 missense variant C/A;T snv 1.2E-05 3
rs63751279 0.925 0.200 16 16150204 missense variant C/T snv 6.0E-05 4.2E-05 5
rs1333662666 1.000 0.160 16 16150640 stop gained C/A;T snv 4.0E-06 4
rs1555506740 1.000 0.160 16 16150774 splice acceptor variant T/G snv 4
rs63751241 0.882 0.280 16 16154638 missense variant C/T snv 4.0E-05 1.4E-05 12
rs66913554 0.882 0.240 16 16154644 stop gained G/A snv 2.0E-05 7.0E-06 7
rs749035807 1.000 0.160 16 16154647 missense variant C/T snv 4.0E-06 7.0E-06 2
rs72664237 1.000 0.160 16 16154732 frameshift variant G/- del 2.8E-05 7
rs63751111 1.000 0.160 16 16154873 missense variant C/G;T snv 8.1E-06 7
rs63750608 1.000 0.160 16 16154889 missense variant A/G snv 8.2E-06 1.4E-05 3
rs63750622 0.925 0.200 16 16154898 missense variant C/A;G;T snv 4.1E-06; 4.1E-06; 1.6E-05 9
rs28939702 0.851 0.320 16 16154899 missense variant G/A;T snv 8.2E-05 13
rs63750414 0.925 0.200 16 16154910 missense variant A/G;T snv 6
rs63750759 0.851 0.280 16 16154974 missense variant G/A;T snv 1.9E-04; 5.4E-06 11
rs63750410 0.882 0.240 16 16155007 missense variant C/G;T snv 6.0E-06; 1.2E-05 9
rs63749856 0.851 0.200 16 16155010 missense variant C/T snv 4.8E-05 2.8E-05 11
rs72664214 1.000 0.160 16 16155037 splice region variant C/G;T snv 5.2E-05 3
rs965791272 1.000 0.160 16 16155041 non coding transcript exon variant G/A;C;T snv 6
rs1297171898 1.000 0.160 16 16157662 splice region variant TCTCTCCT/- delins 5
rs1555507903 1.000 0.160 16 16157716 frameshift variant -/GTCGGTATCTTAG delins 4
rs1555507927 1.000 0.160 16 16157769 frameshift variant -/G ins 4
rs72664233 0.882 0.200 16 16157770 frameshift variant A/- del 8.4E-05 4.9E-05 10
rs63750273 0.851 0.240 16 16157810 splice acceptor variant C/T snv 4.1E-05 1.4E-05 9
rs63749796 0.925 0.200 16 16159505 missense variant C/G snv 9
rs63750125 1.000 0.160 16 16159541 missense variant G/T snv 4