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: rs1261591521
rs1261591521
APOC3
1 1.000 11 116830784 missense variant G/A snv 4.0E-06 0.010 1.000 1 2010 2010
dbSNP: rs752100893
rs752100893
MTTP
1 1.000 4 99581913 missense variant A/G snv 8.0E-06 7.0E-06 0.010 1.000 1 2010 2010