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: rs376892534
rs376892534
6 0.925 0.120 11 103184880 intron variant G/A snv 8.1E-06 0.700 0
dbSNP: rs181011657
rs181011657
3 0.882 0.120 11 103257719 stop gained C/T snv 6.8E-05 1.4E-04 0.700 1.000 1 2017 2017
dbSNP: rs1260978141
rs1260978141
8 1.000 0.120 11 103125293 stop gained C/T snv 4.5E-06 0.700 0
dbSNP: rs1309577378
rs1309577378
1 1.000 0.120 11 103135524 stop gained G/A snv 1.4E-05 0.700 0
dbSNP: rs1565311145
rs1565311145
7 0.882 0.120 11 103116677 stop gained T/A snv 0.700 0
dbSNP: rs1565317399
rs1565317399
6 0.882 0.120 11 103122879 stop gained C/T snv 0.700 0
dbSNP: rs1565423740
rs1565423740
1 1.000 0.120 11 103241546 stop gained G/A snv 0.700 0
dbSNP: rs371011047
rs371011047
9 0.882 0.120 11 103120982 stop gained G/T snv 2.8E-05 0.700 0
dbSNP: rs537704873
rs537704873
1 1.000 0.120 11 103191520 stop gained C/T snv 2.2E-05 1.4E-05 0.700 0
dbSNP: rs562139820
rs562139820
2 0.925 0.120 11 103257731 stop gained C/T snv 1.4E-05 0.700 0
dbSNP: rs754919042
rs754919042
1 1.000 0.120 11 103173242 stop gained C/A;T snv 2.1E-05 0.700 0
dbSNP: rs137853027
rs137853027
15 0.827 0.120 11 103220720 missense variant A/G snv 2.4E-04 2.6E-04 0.700 1.000 4 2009 2018
dbSNP: rs397514637
rs397514637
2 0.925 0.120 11 103117852 missense variant C/T snv 3.2E-05 1.4E-05 0.700 1.000 3 2012 2018
dbSNP: rs1196317554
rs1196317554
1 1.000 0.120 11 103199400 missense variant T/C snv 8.1E-06 5.6E-05 0.700 0
dbSNP: rs1350329646
rs1350329646
2 0.925 0.120 11 103192150 missense variant C/A;T snv 5.1E-06; 5.1E-06 0.700 0
dbSNP: rs137853031
rs137853031
2 0.925 0.120 11 103185032 missense variant G/A snv 4.0E-06 0.700 0
dbSNP: rs1555043520
rs1555043520
2 0.925 0.120 11 103135630 missense variant T/G snv 0.700 0
dbSNP: rs1555052511
rs1555052511
1 1.000 0.120 11 103160971 missense variant T/C snv 0.700 0
dbSNP: rs1555053115
rs1555053115
1 1.000 0.120 11 103163089 missense variant G/A snv 0.700 0
dbSNP: rs1555057838
rs1555057838
1 1.000 0.120 11 103179047 missense variant G/C snv 0.700 0
dbSNP: rs1555081345
rs1555081345
1 1.000 0.120 11 103253347 missense variant T/C snv 0.700 0
dbSNP: rs1555143920
rs1555143920
1 1.000 0.120 11 103479135 missense variant T/C snv 0.700 0
dbSNP: rs189806840
rs189806840
2 0.925 0.120 11 103155439 missense variant C/A snv 1.6E-03 1.8E-03 0.700 0
dbSNP: rs200710887
rs200710887
1 1.000 0.120 11 103253341 missense variant C/A;T snv 3.6E-05; 3.2E-05 0.700 0
dbSNP: rs368631447
rs368631447
2 0.925 0.120 11 103253384 missense variant C/T snv 3.6E-05; 8.0E-06 2.8E-05 0.700 0