Source: ALL
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: rs1454626
rs1454626
VLDLR ; VLDLR-AS1
1 9 2621030 intron variant C/A snv 0.66 0.010 1.000 1 2008 2008
dbSNP: rs1466535
rs1466535
LRP1
9 0.790 0.160 12 57140687 intron variant G/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs2075650
rs2075650
TOMM40
45 0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 0.010 1.000 1 2009 2009
dbSNP: rs3123629
rs3123629
LPAL2
2 6 160485054 intron variant G/A snv 0.28 0.010 1.000 1 2011 2011
dbSNP: rs6065904
rs6065904
PLTP
7 1.000 0.080 20 45906012 intron variant G/A snv 0.23 0.010 1.000 1 2010 2010
dbSNP: rs646776
rs646776
CELSR2
25 0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 0.010 1.000 1 2009 2009