Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1557911386 1.000 0.040 1 151428357 missense variant T/A snv 1
rs1557916296 1.000 0.040 1 151430822 missense variant C/A snv 1
rs1557935477 1.000 0.040 1 151440939 missense variant G/T snv 1
rs1561824498 1.000 0.040 5 88752044 splice acceptor variant C/A snv 1
rs1564801388 1.000 0.040 10 87864353 5 prime UTR variant -/G delins 1
rs1564801473 1.000 0.040 10 87864406 5 prime UTR variant -/C delins 1
rs1564950387 1.000 0.040 11 687909 splice donor variant A/C snv 1
rs1565527302 1.000 0.040 11 70485988 frameshift variant TG/- del 1
rs1569305431 1.000 0.040 X 53254702 frameshift variant G/- delins 1
rs1569513495 1.000 0.040 22 50465238 stop gained C/A snv 1
rs17606561 1.000 0.040 6 10982126 3 prime UTR variant G/A snv 0.17 1
rs202098093 1.000 0.040 1 151405476 missense variant G/A snv 1.2E-05 7.0E-06 1
rs2289195 1.000 0.040 2 25240614 intron variant G/A snv 0.41 0.41 1
rs370498156 1.000 0.040 1 151404903 missense variant T/C;G snv 4.0E-06 1.4E-05 1
rs373783340 1.000 0.040 1 151406243 missense variant G/A snv 4.0E-05 1.2E-04 1
rs375045125 1.000 0.040 1 151429672 missense variant T/C snv 4.0E-06 7.0E-06 1
rs375712202 1.000 0.040 11 124923339 splice donor variant C/T snv 9.6E-05 1.4E-05 1
rs548226228 1.000 0.040 1 151406914 missense variant G/A snv 1.2E-05 2.1E-05 1
rs561369202 1.000 0.040 1 151428152 missense variant T/C snv 6.4E-05 1.4E-05 1
rs574158925 1.000 0.040 1 151427829 missense variant T/C snv 5.6E-05 2.8E-05 1
rs574335012 1.000 0.040 1 151427959 missense variant G/C snv 1.2E-05 1
rs724159978 1.000 0.040 17 30998906 frameshift variant G/- delins 1
rs749270162 1.000 0.040 1 151406620 missense variant T/C snv 2.4E-05 1
rs749548928 1.000 0.040 1 151408815 missense variant T/C;G snv 4.0E-06 1
rs753214391 1.000 0.040 1 151406444 missense variant C/T snv 1.0E-05 2.1E-05 1