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: rs2295080
rs2295080
20 0.695 0.320 1 11262571 upstream gene variant G/C;T snv 0.040 1.000 4 2012 2015
dbSNP: rs1034528
rs1034528
5 0.882 0.120 1 11189075 intron variant G/C snv 0.30 0.010 1.000 1 2016 2016
dbSNP: rs11121704
rs11121704
3 1 11233902 intron variant C/A;T snv 0.010 1.000 1 2014 2014
dbSNP: rs17036508
rs17036508
4 0.925 0.080 1 11195977 3 prime UTR variant T/C snv 9.0E-02 0.010 1.000 1 2016 2016
dbSNP: rs1883965
rs1883965
8 0.807 0.160 1 11262099 intron variant A/G snv 0.63 0.010 1.000 1 2016 2016
dbSNP: rs2295079
rs2295079
4 0.925 0.080 1 11262508 5 prime UTR variant C/G snv 0.54 0.010 < 0.001 1 2019 2019
dbSNP: rs2536
rs2536
11 0.776 0.240 1 11106656 3 prime UTR variant T/C snv 5.8E-02 0.010 1.000 1 2014 2014