Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1346324047
LPA
1.000 0.040 6 160640717 missense variant G/A snv 1
rs772114791
PCSK9
1.000 0.040 1 55052343 missense variant G/A snv 8.0E-06 7.0E-06 1
rs748204991
ST14
1.000 0.040 11 130196396 missense variant G/A snv 2.1E-05 7.0E-06 1
rs12743824 0.925 0.040 1 99317401 intergenic variant C/A snv 0.48 2
rs2862954
ERLIN1
0.925 0.040 10 100152307 missense variant T/C snv 0.34 0.32 2
rs1420472625
MBOAT7
0.925 0.040 19 54178800 missense variant G/C snv 2
rs17007417 0.882 0.080 2 71808541 regulatory region variant T/C snv 0.85 3
rs74315468
ARSA
0.882 0.040 22 50626841 missense variant G/A snv 4.0E-06 2.8E-05 3
rs12137855
LYPLAL1
0.882 0.040 1 219275036 downstream gene variant C/T snv 0.19 3
rs2294918
PNPLA3
0.925 0.040 22 43946236 missense variant A/G snv 0.68 0.70 3
rs2290602
PPARGC1A
0.882 0.040 4 23824109 intron variant T/A;G snv 3
rs738491
SAMM50 ; PNPLA3
0.882 0.040 22 43958231 intron variant C/T snv 0.34 3
rs2070666
APOC3
0.882 0.120 11 116830958 intron variant T/A;C snv 4
rs3213445
CHKB-CPT1B ; CPT1B
0.851 0.120 22 50577409 missense variant T/C snv 0.12 8.9E-02 4
rs12784396
CWF19L1
0.925 0.040 10 100267650 5 prime UTR variant C/A;T snv 4
rs879254597
LDLR
0.851 0.120 19 11105528 stop gained G/A;T snv 4
rs797044485
LMNA
0.851 0.160 1 156134832 missense variant G/A snv 4
rs1010023
PNPLA3
0.851 0.080 22 43940218 intron variant T/C snv 0.20 4
rs951599607
PPARG
0.925 0.040 3 12434028 missense variant G/A snv 4
rs2645424
FDFT1
0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs779021719
HAMP
0.827 0.120 19 35284962 stop gained C/G;T snv 9.1E-05 5
rs4240624
LOC157273
0.882 0.040 8 9326721 intron variant G/A snv 0.87 5
rs2143571
SAMM50
0.827 0.080 22 43995806 intron variant G/A snv 0.25 5
rs56225452
SLC27A5 ; LOC105372486 ; ZBTB45
0.851 0.080 19 58513279 upstream gene variant C/T snv 0.18 5
rs940553638
ALDH2
0.827 0.200 12 111783222 missense variant G/A snv 1.6E-05 7.0E-06 6