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: rs2106261
rs2106261
11 0.763 0.160 16 73017721 intron variant C/G;T snv 0.900 0.929 14 2009 2019
dbSNP: rs7193343
rs7193343
3 0.882 0.120 16 72995261 intron variant T/A;C snv 0.870 0.857 7 2009 2019
dbSNP: rs2359171
rs2359171
1 1.000 0.080 16 73019123 intron variant T/A snv 0.21 0.700 1.000 2 2018 2018
dbSNP: rs4404097
rs4404097
1 1.000 0.080 16 72998133 intron variant G/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs4499262
rs4499262
1 1.000 0.080 16 73025260 intron variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs7190256
rs7190256
16 0.851 0.120 16 72963084 intron variant C/T snv 0.94 0.700 1.000 1 2016 2016
dbSNP: rs876727
rs876727
1 1.000 0.080 16 73033862 intron variant T/G snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs12932445
rs12932445
3 0.925 0.080 16 73035989 intron variant T/C snv 0.18 0.010 1.000 1 2017 2017
dbSNP: rs16971436
rs16971436
4 0.851 0.080 16 72958864 missense variant T/C;G snv 1.2E-05; 7.1E-02 0.010 1.000 1 2014 2014
dbSNP: rs6499600
rs6499600
1 1.000 0.080 16 72945475 intron variant C/T snv 0.51 0.010 1.000 1 2014 2014