Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6746030 0.763 0.320 2 166242648 missense variant A/G snv 0.88 0.88 16
rs121918799 0.752 0.120 2 166015636 missense variant G/C snv 1.7E-03 1.6E-03 14
rs1559193213 0.807 0.160 2 166036149 frameshift variant -/G delins 11
rs121918622 0.790 0.080 2 165992332 missense variant C/A;T snv 4.0E-06 9
rs1553525325 0.807 0.120 2 166002716 missense variant A/T snv 9
rs121917984 0.790 0.080 2 166052869 missense variant G/A;C snv 8
rs3812718 0.776 0.240 2 166053034 splice region variant C/T snv 0.48 8
rs794726827 0.827 0.120 2 166054637 splice donor variant C/A;G;T snv 6
rs121918632 0.851 0.120 2 165996099 missense variant A/G snv 7.0E-06 5
rs121918807 0.851 0.080 2 165994275 missense variant G/A snv 7.2E-05 2.8E-05 5
rs121918628 0.851 0.080 2 165998049 missense variant G/T snv 5
rs121918624 0.827 0.080 2 166052882 stop gained G/A snv 5
rs398123588 0.827 0.080 2 166039436 missense variant C/T snv 8.0E-06 5
rs121918775 0.827 0.080 2 166037886 missense variant G/A;T snv 5
rs121918805 0.925 0.080 2 166002660 missense variant C/A;T snv 2.0E-05 4
rs121918803 0.851 0.040 2 166009745 missense variant C/G snv 4
rs121917953 0.851 0.080 2 166054677 missense variant T/A snv 4
rs398123585 0.851 0.080 2 166043875 stop gained G/A;T snv 4.0E-06 4
rs794726775 0.882 0.040 2 166039420 splice region variant T/A snv 4
rs121917993 0.851 0.040 2 165994212 missense variant G/A snv 4
rs121917918 0.851 0.040 2 166058651 missense variant C/A;T snv 4
rs121917935 0.851 0.040 2 166054660 missense variant C/A;T snv 4
rs121917964 0.851 0.080 2 166073371 missense variant T/C snv 4
rs121917971 0.851 0.080 2 166037885 missense variant C/G;T snv 4
rs6432860 0.925 0.080 2 166041354 synonymous variant A/G;T snv 0.73; 4.0E-06 4