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: rs765696008
rs765696008
4 0.925 0.080 19 11113268 intron variant G/A;C snv 2.8E-05; 4.0E-06 0.700 1.000 9 2001 2015
dbSNP: rs10405652
rs10405652
1 1.000 0.080 19 9630447 intron variant G/T snv 0.13 0.700 1.000 1 2013 2013
dbSNP: rs10411082
rs10411082
1 1.000 0.080 19 9630540 intron variant G/A snv 0.31 0.700 1.000 1 2013 2013
dbSNP: rs10415132
rs10415132
1 1.000 0.080 19 9752807 intron variant G/A snv 0.37 0.700 1.000 1 2013 2013
dbSNP: rs10418705
rs10418705
1 1.000 0.080 19 9658249 intron variant A/G snv 0.27 0.700 1.000 1 2013 2013
dbSNP: rs10422772
rs10422772
1 1.000 0.080 19 9612747 intron variant C/T snv 0.13 0.700 1.000 1 2013 2013
dbSNP: rs10455872
rs10455872
LPA
33 0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 0.010 1.000 1 2019 2019
dbSNP: rs11613352
rs11613352
9 0.827 0.160 12 57398797 intron variant C/T snv 0.19 0.010 1.000 1 2015 2015
dbSNP: rs12526453
rs12526453
5 0.827 0.160 6 12927312 intron variant C/G snv 0.27 0.010 1.000 1 2019 2019
dbSNP: rs12610507
rs12610507
1 1.000 0.080 19 12325596 intron variant A/C snv 0.22 0.700 1.000 1 2013 2013
dbSNP: rs12720762
rs12720762
2 0.925 0.080 2 21043787 intron variant C/G snv 4.8E-03 0.010 1.000 1 2013 2013
dbSNP: rs1333047
rs1333047
9 0.790 0.240 9 22124505 intron variant A/T snv 0.63 0.010 1.000 1 2018 2018
dbSNP: rs1529711
rs1529711
4 1.000 0.080 19 10912758 intron variant C/T snv 0.13 0.700 1.000 1 2013 2013
dbSNP: rs16042
rs16042
1 1.000 0.080 19 13230223 intron variant G/A snv 0.20 0.16 0.700 1.000 1 2013 2013
dbSNP: rs17321515
rs17321515
16 0.776 0.200 8 125474167 intron variant A/G snv 0.49 0.010 1.000 1 2011 2011
dbSNP: rs2033483
rs2033483
1 1.000 0.080 19 9143666 intron variant A/G snv 7.3E-02 0.700 1.000 1 2013 2013
dbSNP: rs2048327
rs2048327
5 0.851 0.120 6 160442500 intron variant T/C snv 0.28 0.010 1.000 1 2019 2019
dbSNP: rs286262
rs286262
1 1.000 0.080 19 11736800 intron variant G/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs2967890
rs2967890
2 1.000 0.080 19 12929833 intron variant G/A snv 0.82 0.700 1.000 1 2013 2013
dbSNP: rs313624
rs313624
1 1.000 0.080 19 11442095 intron variant A/G snv 0.63 0.700 1.000 1 2013 2013
dbSNP: rs370245937
rs370245937
1 1.000 0.080 19 11117009 intron variant C/G;T snv 2.4E-05 0.700 1.000 1 2005 2005
dbSNP: rs3745264
rs3745264
1 1.000 0.080 19 10318890 intron variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs387865
rs387865
1 1.000 0.080 19 11173863 intron variant T/A;C snv 0.700 1.000 1 2013 2013
dbSNP: rs4804149
rs4804149
1 1.000 0.080 19 11173352 intron variant T/C snv 0.32 0.700 1.000 1 2013 2013
dbSNP: rs4804636
rs4804636
1 1.000 0.080 19 11731508 intron variant C/T snv 0.29 0.700 1.000 1 2013 2013