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: rs1057519816
rs1057519816
14 0.763 0.200 17 39711955 missense variant C/A;T snv 0.710 1.000 2 2016 2018
dbSNP: rs1057519787
rs1057519787
2 1.000 0.040 17 39711952 missense variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs1131692237
rs1131692237
2 1.000 0.040 17 39725161 missense variant T/G snv 0.700 0
dbSNP: rs121913469
rs121913469
11 0.763 0.240 17 39723966 missense variant TT/CC mnv 0.700 0
dbSNP: rs397516975
rs397516975
2 0.925 0.080 17 39724728 inframe insertion -/ATACGTGATGGC delins 0.700 0
dbSNP: rs587776805
rs587776805
1 1.000 0.040 17 39724745 inframe insertion -/TGTGGGCTC delins 0.700 0
dbSNP: rs372043866
rs372043866
18 0.732 0.240 17 39727965 missense variant G/A;C;T snv 3.2E-05; 2.4E-05; 1.2E-05 0.070 1.000 7 2008 2018
dbSNP: rs564064363
rs564064363
4 0.851 0.080 17 39706998 missense variant G/A;C snv 1.3E-05 0.010 1.000 1 2017 2017
dbSNP: rs896171398
rs896171398
2 1.000 0.040 17 39709846 missense variant G/A;C snv 1.6E-05 0.010 1.000 1 2017 2017
dbSNP: rs977818812
rs977818812
3 1.000 0.040 17 39723608 missense variant A/T snv 0.010 1.000 1 2014 2014