Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs199476401 0.878 10 68121896 missense variant A/C,G snp 4.0E-06 9.6E-05 2
rs397516881 1.000 10 119676917 missense variant G/A snp 2
rs397517065 15 34792471 missense variant G/A snp 2
rs727505109 1.000 10 119676621 frameshift variant CC/C in-del 2
rs112240298 2 178538945 splice donor variant C/G,T snp 1
rs148894066
DSP
6 7579697 stop gained C/A,T snp 1.4E-04 9.6E-05 1
rs199476310 15 63057019 missense variant T/C snp 1
rs200797552 2 178578078 stop gained C/A,T snp 3.3E-04 6.4E-05 1
rs267607554 1 156135925 stop gained C/T snp 1
rs267607593 1 156134964 missense variant T/C snp 1
rs267607646 1 156115266 frameshift variant G/GG in-del 1
rs368200299 2 178620285 stop gained G/A,T snp 4.9E-06 3.2E-05 1
rs368452607 2 178588700 stop gained G/A,T snp 4.0E-06; 8.0E-06 3.2E-05 1
rs371678190 2 178578066 stop gained G/A,T snp 4.0E-06; 5.6E-05 3.2E-05 1
rs377491278 14 23427773 missense variant C/T snp 1.2E-05 1
rs397515939 11 47339758 stop gained G/A,C snp 8.0E-06 9.6E-05 1
rs397516123 14 23427675 missense variant G/A snp 1
rs397516224 14 23432684 frameshift variant TG/T in-del 4.0E-06 1
rs397516252 14 23413832 missense variant G/C snp 1
rs397516253 14 23413823 missense variant C/G,T snp 1.2E-05 1
rs397516352 19 55154115 missense variant A/G snp 1
rs397516355 19 55154035 missense variant C/A,T snp 1
rs397516356 19 55151917 missense variant C/T snp 1
rs397516363 15 63044075 missense variant G/A snp 1
rs397516369 15 63057081 missense variant C/G snp 1