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: rs111033567
rs111033567
3 0.882 0.040 7 142750582 missense variant A/G snv 0.010 1.000 1 2015 2015
dbSNP: rs376907511
rs376907511
1 1.000 0.040 7 142752517 missense variant A/G snv 6.4E-05 0.010 < 0.001 1 2010 2010
dbSNP: rs1800080
rs1800080
2 0.925 0.120 7 117534330 missense variant A/G snv 0.010 < 0.001 1 2010 2010
dbSNP: rs886037774
rs886037774
LPL
7 0.882 0.120 8 19955993 missense variant T/C snv 0.010 1.000 1 2017 2017
dbSNP: rs886037775
rs886037775
LPL
7 0.882 0.120 8 19960948 missense variant A/T snv 0.010 1.000 1 2017 2017
dbSNP: rs1223231582
rs1223231582
24 0.677 0.280 7 142750639 missense variant A/G snv 7.0E-06 0.020 1.000 2 2006 2014
dbSNP: rs17107315
rs17107315
40 0.620 0.440 5 147828115 missense variant T/C snv 9.1E-03 8.2E-03 0.060 0.667 6 2006 2014