Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs137852569
rs137852569
AR
10 0.752 0.320 X 67686030 missense variant G/A snv 9.4E-06 0.700 0
dbSNP: rs137852577
rs137852577
AR
3 0.882 0.200 X 67722898 missense variant C/T snv 0.700 0
dbSNP: rs137852590
rs137852590
AR
1 1.000 0.160 X 67545667 stop gained T/G snv 0.700 0
dbSNP: rs141425171
rs141425171
AR
3 1.000 0.160 X 67717574 missense variant A/G;T snv 2.2E-05; 5.5E-06 0.700 0
dbSNP: rs142280455
rs142280455
AR
1 1.000 0.160 X 67686033 missense variant A/G snv 3.1E-04 3.8E-04 0.700 0
dbSNP: rs1555982894
rs1555982894
AR
2 0.925 0.160 X 67643409 splice donor variant T/C snv 0.700 0
dbSNP: rs201934623
rs201934623
AR
2 0.925 0.160 X 67546320 missense variant C/T snv 4.5E-03 2.0E-03 0.700 0
dbSNP: rs886041352
rs886041352
AR
2 0.925 0.160 X 67717618 missense variant A/C snv 0.700 0
dbSNP: rs9332971
rs9332971
AR
4 0.851 0.200 X 67722944 missense variant G/A;T snv 0.700 0