Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137852589
AR
0.925 0.160 X 67721857 missense variant G/A;T snv 5.5E-06 2
rs137852591
AR
0.851 0.200 X 67721909 missense variant C/G snv 1.4E-03 1.4E-03 4
rs137852594
AR
1.000 0.160 X 67723745 synonymous variant C/T snv 1
rs137852595
AR
0.925 0.160 X 67711653 missense variant C/A;T snv 2
rs137852596
AR
1.000 0.160 X 67643371 missense variant G/A snv 1
rs137852597
AR
1.000 0.160 X 67722973 missense variant T/C snv 1
rs137852598
AR
1.000 0.160 X 67722948 missense variant C/G;T snv 5.5E-06 1
rs137852599
AR
1.000 0.160 X 67711585 missense variant A/C snv 1
rs137852600
AR
0.925 0.160 X 67717535 missense variant G/A;T snv 2
rs1386577803
AR
0.851 0.240 X 67722872 missense variant G/A snv 4
rs139524801
AR
0.925 0.160 X 67643283 missense variant G/A;T snv 1.8E-04 3
rs1410383824
AR
0.925 0.160 X 67546470 stop gained G/A;T snv 2
rs143040492
AR
0.882 0.200 X 67723690 missense variant C/T snv 1.1E-05 9.6E-06 3
rs1481151440
AR
1.000 0.160 X 67545467 stop gained C/A;T snv 1
rs1555969512
AR
1.000 0.160 X 67545360 stop gained C/T snv 1
rs1555969545
AR
1.000 0.160 X 67545414 stop gained C/T snv 1
rs1555969553
AR
0.925 0.200 X 67545438 stop gained C/T snv 2
rs1555969682
AR
1.000 0.160 X 67545889 missense variant G/T snv 1
rs1555969684
AR
0.925 0.200 X 67545892 frameshift variant -/G delins 2
rs1555969694
AR
1.000 0.160 X 67545936 frameshift variant -/G delins 1
rs1555969807
AR
1.000 0.160 X 67546331 stop gained C/A snv 1
rs1555970004
AR
0.925 0.200 X 67546581 frameshift variant -/C delins 2
rs1555982860
AR
1.000 0.160 X 67643327 missense variant G/A snv 1
rs1555982894
AR
0.925 0.160 X 67643409 splice donor variant T/C snv 2
rs1555990470
AR
0.925 0.200 X 67686046 missense variant G/A snv 2