Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1566174147 1.000 0.080 13 48304003 frameshift variant -/A delins 1
rs1566186087
RB1
1.000 0.080 13 48342631 frameshift variant -/A ins 1
rs1566234123
RB1
1.000 0.080 13 48456342 frameshift variant -/A delins 1
rs587778828 1.000 0.080 13 48364911 frameshift variant -/A delins 1
rs1555294600
RB1
1.000 0.080 13 48465033 frameshift variant -/AA ins 1
rs1555285429 1.000 0.080 13 48367532 stop gained -/AAAAATAAAGATCTAGATGCAAGATTATTTTTGGATCATGATAAAACTCTTCAGA delins 1
rs1555283670
RB1
1.000 0.080 13 48349012 stop gained -/ATTAG delins 1
rs1131690852 1.000 0.080 13 48303925 frameshift variant -/C delins 2
rs587778830 1.000 0.080 13 48373422 frameshift variant -/C delins 1
rs587778851
RB1
1.000 0.080 13 48476704 frameshift variant -/C delins 1
rs1566233014
RB1
1.000 0.080 13 48453034 frameshift variant -/G delins 1
rs587776790 1.000 0.080 13 48303953 frameshift variant -/GCTGCCGCCGCGGAACCCCCGGC delins 1
rs1555279212 1.000 0.080 13 48303958 frameshift variant -/GGAACCCCCGGCACCGCCGC delins 1
rs1555279210 1.000 0.080 13 48303957 frameshift variant -/GGAACCCCCGGCACCGCCGCCGC delins 2
rs1555286236 1.000 0.080 13 48376977 frameshift variant -/T delins 1
rs1566237098
RB1
1.000 0.080 13 48463794 frameshift variant -/T delins 1
rs587778854
RB1
1.000 0.080 13 48345161 frameshift variant -/T delins 1
rs587778824
RB1
1.000 0.080 13 48307368 frameshift variant -/TA delins 1
rs70991108 0.807 0.280 5 80654344 intron variant -/TCGCGCGTCCCGCCCAGGT;TGGCGCGTCCCGCCCAGGT ins 0.51 6
rs1555286707 1.000 0.080 13 48381420 frameshift variant -/TG delins 1
rs1566186889
RB1
1.000 0.080 13 48345163 stop gained -/TGAT delins 1
rs587778836
RB1
1.000 0.080 13 48465012 frameshift variant -/TGAT delins 1
rs1566174074 1.000 0.080 13 48303952 frameshift variant -/TGCCGCCGCGGAACCCCCGGCACCGC delins 1
rs1131690901 1.000 0.080 13 48364897 frameshift variant A/- delins 2
rs587778844 1.000 0.080 13 48367575 frameshift variant A/- delins 2