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: rs118204057
rs118204057
LPL
16 0.732 0.400 8 19954222 missense variant G/A;C snv 1.9E-04 0.010 1.000 1 1998 1998
dbSNP: rs118204060
rs118204060
LPL
9 0.807 0.160 8 19954279 missense variant C/T snv 4.0E-05 1.4E-05 0.010 1.000 1 1998 1998
dbSNP: rs200353509
rs200353509
APOB
4 0.882 0.120 2 21035701 missense variant G/A;C;T snv 4.0E-06; 6.0E-05 0.010 1.000 1 1998 1998
dbSNP: rs268
rs268
LPL
41 0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 0.010 1.000 1 1998 1998
dbSNP: rs753248521
rs753248521
LDLR ; MIR6886
4 0.882 0.120 19 11111523 missense variant A/G snv 4.0E-06 0.010 1.000 1 1998 1998
dbSNP: rs879254642
rs879254642
LDLR
6 0.882 0.120 19 11105589 missense variant A/C;G snv 0.010 1.000 1 1998 1998
dbSNP: rs879254851
rs879254851
LDLR ; MIR6886
6 0.882 0.120 19 11113368 missense variant T/C snv 0.010 1.000 1 1998 1998