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: rs113298164
rs113298164
LIPC
1 1.000 0.040 15 58563549 missense variant C/T snv 2.9E-03 2.9E-03 0.800 0
dbSNP: rs121912502
rs121912502
LIPC
2 0.925 0.080 15 58548387 missense variant C/T snv 1.0E-03 7.5E-04 0.710 1.000 3 1991 1998
dbSNP: rs1566946168
rs1566946168
LIPC
1 1.000 0.040 15 58545750 missense variant G/A snv 0.700 0
dbSNP: rs202215798
rs202215798
LIPC
1 1.000 0.040 15 58560960 missense variant T/C snv 1.6E-05 1.4E-05 0.010 1.000 1 1991 1991