Gene: LPL ×
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: rs268
rs268
LPL
41 0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 0.800 1.000 1 2012 2012
dbSNP: rs295
rs295
LPL
1 1.000 0.040 8 19958727 intron variant A/C snv 0.28 0.800 1.000 1 2011 2011
dbSNP: rs301
rs301
LPL
7 0.925 0.160 8 19959423 intron variant T/C snv 0.24 0.26 0.800 1.000 1 2011 2011
dbSNP: rs263
rs263
LPL
4 1.000 0.040 8 19955301 intron variant C/T snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs271
rs271
LPL
4 1.000 0.040 8 19956191 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs328
rs328
LPL
19 0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 0.020 0.500 2 2015 2015
dbSNP: rs965384857
rs965384857
LPL
5 0.827 0.160 8 19954234 missense variant G/A snv 4.0E-06 0.010 1.000 1 2018 2018