Source: CLINVAR

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs202067416 1.000 12 8868358 splice donor variant G/A;C snv 9.9E-04 1.1E-03 1
rs778598915 1.000 0.080 22 42693910 synonymous variant G/A;T snv 2.2E-05 1
rs397514502 1.000 22 42693321 missense variant G/C snv 1
rs121918550 1.000 0.080 12 53309624 missense variant A/G snv 1.2E-04 4.9E-05 5
rs121918549 0.882 0.080 12 53321423 stop gained G/A;T snv 4.0E-06; 1.8E-04 5
rs770214071 1.000 0.080 12 53308469 frameshift variant CAGA/- delins 2.8E-05 7.7E-05 1
rs1035139364 1.000 0.080 12 53308724 splice donor variant C/T snv 7.0E-06 1
rs1565781382 1.000 0.080 12 53315142 splice acceptor variant T/C snv 1
rs754637718 1.000 0.080 12 53320565 stop gained C/T snv 4.4E-05 2.8E-05 1
rs121918551 0.882 0.200 12 53308095 missense variant G/A snv 4.0E-06 1
rs121918547 1.000 0.080 12 53309158 stop gained G/A;C snv 1.6E-05; 4.0E-06; 4.0E-06 1
rs150511103 1.000 0.080 12 53308051 splice donor variant C/A;G;T snv 4.0E-06; 4.0E-06; 4.8E-05 1
rs773601814 1.000 0.080 12 53309018 missense variant A/G;T snv 4.0E-06 1
rs121918548 1.000 0.080 12 53307698 stop gained G/A snv 4.0E-05 7.7E-05 1
rs387906326 1.000 0.080 12 53308975 frameshift variant -/A delins 1
rs1567027610 1.000 0.080 15 67236690 frameshift variant GAAA/- delins 1
rs753247583 1.000 0.080 15 67203547 splice donor variant C/T snv 1.6E-05 1.4E-05 1
rs200564757 0.925 0.080 15 67236060 stop gained G/A;T snv 2.0E-05 1
rs781596375 1.000 0.080 15 67231876 frameshift variant C/- delins 1
rs746488412 0.925 0.080 15 67231868 stop gained G/A snv 8.0E-06 1
rs1567027297 1.000 0.080 15 67236420 frameshift variant CT/- delins 1
rs1057518846 1.000 0.080 15 67235978 splice donor variant C/A;G snv 1
rs746800707 0.851 0.160 20 36240388 missense variant G/A;C;T snv 1.2E-05; 4.0E-06 8
rs267606621 0.882 0.080 16 70268356 missense variant C/T snv 3
rs797044801 1.000 0.080 16 70254688 missense variant T/G snv 1