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: rs11542041
rs11542041
23 0.677 0.480 19 44908690 missense variant C/A;T snv 2.1E-05 0.030 1.000 3 1995 2001
dbSNP: rs573658040
rs573658040
9 0.790 0.200 19 44908705 missense variant C/G;T snv 6.3E-06 0.020 1.000 2 1996 2006
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 1995 1995
dbSNP: rs121918397
rs121918397
3 0.882 0.200 19 44908784 missense variant G/A;C snv 6.5E-06 0.010 1.000 1 2001 2001
dbSNP: rs198388
rs198388
4 0.851 0.160 1 11857283 downstream gene variant C/G;T snv 0.010 1.000 1 2014 2014
dbSNP: rs198389
rs198389
10 0.776 0.240 1 11859214 upstream gene variant A/G snv 0.39 0.010 1.000 1 2014 2014
dbSNP: rs387906567
rs387906567
4 0.882 0.200 19 44908774 missense variant C/G;T snv 6.3E-06 0.010 1.000 1 2011 2011
dbSNP: rs5742904
rs5742904
22 0.689 0.280 2 21006288 missense variant C/A;T snv 2.8E-04 7.3E-04 0.010 1.000 1 1992 1992
dbSNP: rs632793
rs632793
3 0.882 0.120 1 11850620 upstream gene variant A/G snv 0.45 0.010 1.000 1 2014 2014
dbSNP: rs769455
rs769455
8 0.827 0.120 19 44908783 missense variant C/T snv 1.4E-03 6.9E-03 0.010 1.000 1 2006 2006
dbSNP: rs879254693
rs879254693
7 0.807 0.160 19 11107424 missense variant T/A;C;G snv 0.010 1.000 1 2001 2001