Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7775478
EYS
1.000 0.040 6 65151300 intron variant G/T snv 0.26 1
rs2920283
JRK ; PSCA
0.925 0.040 8 142675619 intron variant T/C snv 0.44 2
rs16896391
EYS
1.000 0.040 6 65196105 intron variant T/C snv 0.23 1
rs28473387 1.000 0.040 8 142626112 intergenic variant T/C snv 0.63 1
rs7046863 1.000 0.040 9 133246054 downstream gene variant T/C snv 0.27 1
rs9297976
JRK ; PSCA
0.790 0.160 8 142670817 intron variant T/C;G snv 7
rs1036385 1.000 0.040 8 142761483 upstream gene variant T/C;G snv 1
rs2244163 1.000 0.040 8 142703082 3 prime UTR variant T/G snv 0.42 0.43 1