Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs137852564
AR
0.827 0.240 X 67722976 missense variant G/A;T snv 5
rs137852573
AR
0.807 0.280 X 67686064 missense variant G/A snv 4
rs137852569
AR
0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 3
rs137852577
AR
0.882 0.200 X 67722898 missense variant C/T snv 3
rs137852591
AR
0.851 0.200 X 67721909 missense variant C/G snv 1.4E-03 1.4E-03 3
rs143040492
AR
0.882 0.200 X 67723690 missense variant C/T snv 1.1E-05 9.6E-06 3
rs886041133
AR
0.882 0.200 X 67723746 missense variant G/A;C snv 5.5E-06 3
rs9332969
AR
0.827 0.240 X 67722899 missense variant G/A;T snv 3
rs9332971
AR
0.851 0.200 X 67722944 missense variant G/A;T snv 3
rs1085307685
AR
0.925 0.160 X 67717552 missense variant A/G snv 2
rs112374098
AR
0.925 0.200 X 67545417 stop gained C/A;T snv 2
rs137852565
AR
0.925 0.200 X 67721905 stop gained G/A;C snv 5.5E-06 2
rs137852572
AR
0.925 0.160 X 67721838 missense variant G/A snv 2
rs137852587
AR
0.925 0.160 X 67643387 missense variant T/A snv 2
rs137852588
AR
0.925 0.160 X 67643284 missense variant C/T snv 2
rs137852589
AR
0.925 0.160 X 67721857 missense variant G/A;T snv 5.5E-06 2
rs137852595
AR
0.925 0.160 X 67711653 missense variant C/A;T snv 2
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 2
rs1555969553
AR
0.925 0.200 X 67545438 stop gained C/T snv 2
rs1555969684
AR
0.925 0.200 X 67545892 frameshift variant -/G delins 2
rs1555970004
AR
0.925 0.200 X 67546581 frameshift variant -/C delins 2
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
rs1555995822
AR
0.925 0.200 X 67711569 missense variant G/A snv 2