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: rs121964882
rs121964882
AVP
1 1.000 0.120 20 3083037 missense variant C/T snv 0.800 1.000 20 1992 2004
dbSNP: rs121964883
rs121964883
AVP
1 1.000 0.120 20 3083156 missense variant C/A snv 0.800 1.000 20 1992 2004
dbSNP: rs121964885
rs121964885
AVP
1 1.000 0.120 20 3083022 missense variant C/A snv 0.800 1.000 20 1992 2004
dbSNP: rs121964886
rs121964886
AVP
1 1.000 0.120 20 3083012 missense variant C/A snv 0.800 1.000 20 1992 2004
dbSNP: rs121964887
rs121964887
AVP
1 1.000 0.120 20 3083138 missense variant C/A snv 0.800 1.000 20 1992 2004
dbSNP: rs121964888
rs121964888
AVP
1 1.000 0.120 20 3083139 missense variant C/G snv 0.800 1.000 20 1992 2004
dbSNP: rs121964890
rs121964890
AVP
1 1.000 0.120 20 3083039 missense variant G/A snv 0.800 1.000 20 1992 2004
dbSNP: rs121964891
rs121964891
AVP
1 1.000 0.120 20 3083024 missense variant C/T snv 0.800 1.000 20 1992 2004
dbSNP: rs121964893
rs121964893
AVP
2 0.925 0.120 20 3084614 missense variant A/G snv 0.800 1.000 20 1992 2004
dbSNP: rs142886338
rs142886338
AVP
1 1.000 0.120 20 3084598 missense variant G/A snv 1.2E-05 7.0E-06 0.700 1.000 20 1992 2004
dbSNP: rs28934878
rs28934878
AVP
1 1.000 0.120 20 3083099 missense variant A/G snv 0.800 1.000 20 1992 2004
dbSNP: rs387906511
rs387906511
AVP
1 1.000 0.120 20 3084620 missense variant C/T snv 0.800 1.000 20 1992 2004
dbSNP: rs387906512
rs387906512
AVP
1 1.000 0.120 20 3084619 missense variant G/A snv 0.800 1.000 20 1992 2004
dbSNP: rs74315383
rs74315383
AVP
1 1.000 0.120 20 3082779 missense variant A/C snv 0.800 1.000 20 1992 2004
dbSNP: rs1232197674
rs1232197674
5 0.827 0.240 6 50838070 missense variant C/T snv 4.0E-06 1.4E-05 0.010 1.000 1 2019 2019
dbSNP: rs2243250
rs2243250
IL4
61 0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 0.010 1.000 1 2014 2014
dbSNP: rs4073
rs4073
64 0.566 0.800 4 73740307 upstream gene variant A/T snv 0.46 0.010 1.000 1 2014 2014
dbSNP: rs1057516192
rs1057516192
AVP
1 1.000 0.120 20 3083168 missense variant C/A snv 0.700 0
dbSNP: rs121964884
rs121964884
AVP
4 0.851 0.200 20 3083005 stop gained G/A;T snv 0.700 0
dbSNP: rs121964889
rs121964889
AVP
1 1.000 0.120 20 3082788 stop gained C/A;T snv 0.700 0
dbSNP: rs770374710
rs770374710
87 0.611 0.560 15 23645747 frameshift variant G/-;GG delins 0.700 0