Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs76763715
GBA
0.658 0.520 1 155235843 missense variant T/C;G snv 2.3E-03 35
rs1289324472
GBA
0.716 0.400 1 155236354 missense variant T/C snv 1.4E-05 21
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 9
rs1264352930
APOA1 ; APOA1-AS
0.807 0.120 11 116836082 missense variant C/A snv 4.2E-06 6
rs2294213
PLTP
0.925 0.080 20 45912053 intron variant C/A;G snv 2
rs1475982887
APOB
1.000 0.080 2 21032489 missense variant A/G snv 4.0E-06 1
rs1160100323
LCAT
1.000 0.080 16 67939938 missense variant G/A snv 7.0E-06 1