Disease: Androgen-Insensitivity Syndrome
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
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
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
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
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
rs1555996810
AR
0.925 0.200 X 67717480 missense variant T/C snv 2
rs1555996863
AR
0.925 0.200 X 67717600 missense variant G/A snv 2
rs1555997580
AR
0.925 0.200 X 67721873 stop gained C/T snv 2
rs1555998108
AR
0.925 0.200 X 67723776 missense variant A/T snv 2
rs1569263557
AR
0.925 0.200 X 67545341 stop gained GCAGC/TT delins 2
rs1569264288
AR
0.925 0.200 X 67545971 frameshift variant -/CCGCTGTGCGTCCCAC delins 2
rs1569265331
AR
0.925 0.200 X 67546597 frameshift variant CTCG/- del 2
rs1569265470
AR
0.925 0.200 X 67546759 frameshift variant -/G delins 2
rs1569314508
AR
0.925 0.200 X 67717623 splice donor variant G/C snv 2