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: rs10455872
rs10455872
LPA
10 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.770 0.875 1 2012 2019
dbSNP: rs41272114
rs41272114
LPA
2 1.000 0.040 6 160585045 splice donor variant C/A;T snv 1.2E-05; 4.1E-02 0.710 1.000 1 2014 2018
dbSNP: rs74617384
rs74617384
LPA
5 0.925 0.080 6 160576086 intron variant A/G;T snv 0.710 1.000 1 2018 2018
dbSNP: rs55730499
rs55730499
LPA
2 1.000 0.040 6 160584578 intron variant C/T snv 4.5E-02 0.700 1.000 3 2015 2018
dbSNP: rs140570886
rs140570886
LPA
3 1.000 0.040 6 160591981 intron variant T/C snv 2.8E-02 0.700 1.000 2 2017 2018
dbSNP: rs73596816
rs73596816
LPA
2 1.000 0.040 6 160596331 intron variant G/A snv 3.6E-02 0.700 1.000 2 2018 2019
dbSNP: rs6926458
rs6926458
LPA
2 1.000 0.040 6 160598834 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs7770628
rs7770628
LPA
2 1.000 0.040 6 160597142 intron variant C/T snv 0.63 0.700 1.000 1 2019 2019