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 0.830 1.000 6 2011 2018
dbSNP: rs3798220
rs3798220
LPA
16 0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 0.820 1.000 4 2011 2013
dbSNP: rs7767084
rs7767084
LPA
2 0.925 0.040 6 160541471 intron variant T/C snv 0.13 0.710 1.000 2 2009 2013
dbSNP: rs10755578
rs10755578
LPA
2 0.925 0.040 6 160548706 intron variant C/G snv 0.44 0.42 0.700 1.000 1 2009 2009