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 0.800 1.000 12 2009 2019
dbSNP: rs2075290
rs2075290
10 0.882 0.160 11 116782580 intron variant C/G;T snv 0.800 1.000 4 2011 2019
dbSNP: rs2266788
rs2266788
19 0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 0.800 1.000 3 2011 2018
dbSNP: rs12286037
rs12286037
6 1.000 0.040 11 116781491 intron variant C/T snv 0.11 0.800 1.000 2 2012 2019
dbSNP: rs2075291
rs2075291
15 0.752 0.400 11 116790676 missense variant C/A;T snv 6.4E-03; 4.0E-06 0.700 1.000 3 2018 2019
dbSNP: rs11604424
rs11604424
4 11 116780399 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12285095
rs12285095
4 11 116787315 non coding transcript exon variant T/G snv 9.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs2072560
rs2072560
5 11 116791110 missense variant T/C snv 0.89 0.94 0.700 1.000 1 2012 2012
dbSNP: rs2160669
rs2160669
5 1.000 0.040 11 116776891 3 prime UTR variant C/T snv 0.92 0.700 1.000 1 2019 2019
dbSNP: rs3741297
rs3741297
2 11 116786951 intron variant C/T snv 8.6E-03 1.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs3741298
rs3741298
5 11 116786845 intron variant C/T snv 0.73 0.700 1.000 1 2018 2018
dbSNP: rs6589566
rs6589566
10 0.882 0.080 11 116781707 intron variant G/A;C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs7483863
rs7483863
1 11 116781775 intron variant A/G snv 0.93 0.700 1.000 1 2018 2018