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: rs652438
rs652438
14 0.716 0.400 11 102865911 missense variant T/C;G snv 7.1E-02; 2.5E-04 0.040 1.000 4 2010 2018
dbSNP: rs2276109
rs2276109
18 0.701 0.440 11 102875061 upstream gene variant T/C snv 9.2E-02 0.020 0.500 2 2017 2019
dbSNP: rs1422753499
rs1422753499
2 0.925 0.120 11 102873034 missense variant T/C;G snv 7.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs371800506
rs371800506
1 1.000 0.040 11 102873067 missense variant C/G snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs56184183
rs56184183
1 1.000 0.040 11 102863081 3 prime UTR variant A/C snv 1.1E-03 1.0E-03 0.010 1.000 1 2012 2012
dbSNP: rs782759740
rs782759740
1 1.000 0.040 11 102873055 stop gained T/A;C snv 4.0E-06 0.010 1.000 1 2010 2010