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: rs964184
rs964184
47 0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 0.810 1.000 1 2012 2012
dbSNP: rs12286037
rs12286037
6 1.000 0.040 11 116781491 intron variant C/T snv 0.11 0.800 1.000 1 2011 2011
dbSNP: rs2075290
rs2075290
10 0.882 0.160 11 116782580 intron variant C/G;T snv 0.800 1.000 1 2011 2011
dbSNP: rs2266788
rs2266788
19 0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 0.800 1.000 1 2011 2011
dbSNP: rs2075291
rs2075291
15 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 0.720 1.000 3 2008 2019
dbSNP: rs6589566
rs6589566
10 0.882 0.080 11 116781707 intron variant G/A;C;T snv 0.710 1.000 2 2014 2018
dbSNP: rs603446
rs603446
2 1.000 0.040 11 116783719 intron variant C/T snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs121917821
rs121917821
2 0.925 0.080 11 116790814 stop gained G/A snv 4.0E-06 0.010 1.000 1 2018 2018
dbSNP: rs2160669
rs2160669
5 1.000 0.040 11 116776891 3 prime UTR variant C/T snv 0.92 0.010 1.000 1 2019 2019
dbSNP: rs7118999
rs7118999
1 1.000 0.040 11 116774559 3 prime UTR variant C/A;T snv 0.010 1.000 1 2017 2017