Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs1380576
MDM4
0.763 0.240 1 204519150 intron variant G/C snv 0.57 10
rs70991108
MSH3 ; DHFR
0.807 0.280 5 80654344 intron variant -/TCGCGCGTCCCGCCCAGGT;TGGCGCGTCCCGCCCAGGT ins 0.51 6
rs2270744
MYH10
1.000 0.080 17 8490582 intron variant G/C snv 0.36 0.35 3
rs1074182
RBL2
1.000 0.080 16 53437445 intron variant T/G snv 0.55 2
rs587781256
LOC112268118 ; RB1
1.000 0.080 13 48380087 intron variant ACTTTTAGTAAAAAATTTTTT/- delins 2
rs9568036
LPAR6 ; RB1
1.000 0.080 13 48397800 intron variant G/A;T snv 2
rs1060503088
RB1
1.000 0.080 13 48452981 intron variant T/G snv 1
rs427686
RB1
1.000 0.080 13 48384180 intron variant C/T snv 0.77 1
rs587776791
RB1
1.000 0.080 13 48471962 intron variant A/G snv 1
rs9535023
LOC112268118 ; RB1
1.000 0.080 13 48380039 intron variant A/G;T snv 4.2E-02 1
rs121913304
RB1 ; LOC112268118
0.925 0.080 13 48381414 stop gained C/T snv 4
rs1060503079
RB1 ; LOC112268118
1.000 0.080 13 48377030 stop gained C/A snv 2
rs1131690863
RB1
1.000 0.080 13 48362847 stop gained C/T snv 2
rs1131690908
RB1
1.000 0.080 13 48473383 stop gained C/A;G snv 2
rs121913296
RB1
1.000 0.080 13 48345108 stop gained G/T snv 2
rs121913300
LOC112268118 ; RB1
1.000 0.080 13 48367512 stop gained C/G;T snv 1.2E-05 2
rs121913301
LOC112268118 ; RB1
1.000 0.080 13 48368549 stop gained C/T snv 2
rs121913302
RB1 ; LOC112268118
1.000 0.080 13 48379624 stop gained C/T snv 7.0E-06 2
rs121913303
RB1 ; LOC112268118
1.000 0.080 13 48381402 stop gained C/T snv 2
rs121913305
RB1
1.000 0.080 13 48453032 stop gained C/T snv 2
rs137853293
RB1
1.000 0.080 13 48465238 stop gained C/T snv 2
rs3092891
RB1 ; LOC112268118
1.000 0.080 13 48379594 stop gained C/T snv 4.0E-06 2
rs398123331
LOC112268118 ; RB1
1.000 0.080 13 48380062 stop gained C/A;G;T snv 7.6E-06 2
rs587778842
RB1
1.000 0.080 13 48362859 stop gained C/T snv 2