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
33 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.800 1.000 6 2012 2019
dbSNP: rs191555775
rs191555775
LPA
3 6 160584357 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs3798220
rs3798220
LPA
16 0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs74617384
rs74617384
LPA
5 0.925 0.080 6 160576086 intron variant A/G;T snv 0.700 1.000 1 2019 2019