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: rs121909293
rs121909293
1 0.851 0.080 1 15445717 missense variant C/T snv 4.4E-03 3.8E-03 0.800 1.000 4 2008 2015
dbSNP: rs142560329
rs142560329
1 0.925 0.040 1 15445703 missense variant C/T snv 9.9E-05 2.2E-04 0.700 1.000 4 2008 2013
dbSNP: rs200678111
rs200678111
1 1.000 0.040 1 15444645 missense variant A/G snv 7.8E-04 9.1E-05 0.700 1.000 4 2008 2013
dbSNP: rs202058123
rs202058123
1 1.000 0.040 1 15445606 missense variant G/A;C snv 6.0E-05 0.700 1.000 4 2008 2013
dbSNP: rs140993290
rs140993290
1 1.000 0.040 1 15445660 missense variant G/A snv 1.1E-03 4.2E-04 0.700 0