Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1555955061
CHM
X 85965588 intron variant T/C snv 2
rs1556300621 X 107645286 missense variant C/T snv 2
rs758291149 3 101244651 stop gained A/G;T snv 2.4E-05 2.1E-05 2
rs867288458 X 107645287 missense variant G/A;C snv 2
rs1064793014 1 94007707 missense variant T/C snv 1
rs111733491 2 169236027 missense variant C/A;G;T snv 8.0E-06; 3.6E-05 1
rs1189889920 3 121790208 stop gained G/A snv 7.0E-06 1
rs1196489060 4 16018318 splice region variant C/T snv 4.0E-06 1.4E-05 1
rs1356104318 1 94098850 stop gained G/A;C snv 4.0E-06 1
rs137853907 4 16000517 stop gained G/T snv 2.8E-05 8.4E-05 1
rs1401818080 8 43197027 splice region variant -/A delins 4.0E-06; 1.2E-05 1.4E-05 1
rs1435861529
EYS ; PHF3
6 63762538 missense variant C/T snv 2.1E-05 1
rs149071415 1 94047024 missense variant A/G snv 4.0E-05 8.4E-05 1
rs1553190559 1 94042790 missense variant A/T snv 1
rs1553192432 1 94060712 frameshift variant -/C delins 1
rs1553249226 1 197328605 missense variant G/A snv 1
rs1553263218 1 197435404 frameshift variant -/G delins 1
rs1553403585 2 73449482 frameshift variant -/CTATTCTGGACTG ins 1
rs1553512879 2 181544799 splice region variant G/C snv 1
rs1553711564 3 121788283 splice donor variant C/T snv 1
rs1554186385 6 42178410 missense variant A/C snv 1
rs1554214453
EYS
6 64886713 stop gained A/T snv 1
rs1554270834 6 42722069 frameshift variant GCTGGGTC/- del 1
rs1554628460 9 2717843 frameshift variant -/GTTCCGGCTCCCAGGCCAGCATCCACGGCTGGACAGAGGGCAACTATAACTACTACATCGAGGAAGACGAAGACGGCGAGGAGGAGGACCAGTGGAAGGACGACCTGGCAGAAGAGGACCAGCAGGCAGGGGAGGTCACCACCGCCAAGCCCGAGGGCCCCAGCGACCCTCCGGCCCTGCTGTCC delins 1
rs1554824273
RGR
10 84258712 3 prime UTR variant -/G delins 1