Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6982636 8 125467073 intron variant G/A snv 0.43 7
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 7
rs7499892
CETP
16 56972678 intron variant C/G;T snv 7
rs863750
ZNF664-RFLNA ; RFLNA
12 124020897 intron variant C/T snv 0.53 7
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs1041968
APOB
2 21009932 synonymous variant G/A snv 0.39 0.38 6
rs10761731
JMJD1C
10 63267850 intron variant A/T snv 0.38 6
rs112259268 17 43797377 downstream gene variant C/A snv 1.9E-02 6
rs11568746
TGFBR1
9 99105926 intron variant C/G snv 2.1E-05 6
rs11571151
PGR-AS1 ; PGR
11 101127486 missense variant C/G;T snv 6
rs12720922
CETP
16 56966973 intron variant G/A snv 0.23 6
rs127430
APCDD1L-DT
20 58589799 intron variant A/G;T snv 6
rs1358980
LOC105375070
6 43796814 intergenic variant C/T snv 0.40 6
rs17240378
LCAT
16 67942790 intron variant G/C;T snv 4.0E-06 6
rs174551
FADS1 ; FADS2
11 61806212 5 prime UTR variant T/C snv 0.28 6
rs1874148
VCL
10 74114657 intron variant A/G snv 1.8E-02 6
rs2169387
LOC157273
8 9323885 intron variant A/G snv 0.87 6
rs2230667
IRF3
19 49662445 missense variant C/T snv 1.0E-04 1.4E-05 6
rs2642438
MTARC1
1 220796686 missense variant A/G snv 0.75 0.78 6
rs2980869 8 125476008 intron variant C/T snv 0.48 6
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs2980880 8 125468730 intron variant G/A snv 0.69 6
rs3093267
F7
13 113118661 missense variant G/A;T snv 8.0E-05 6
rs33980385
CYP2B6
19 40991388 missense variant A/G snv 6
rs34090729
RXRA
9 134401999 non coding transcript exon variant C/T snv 1.6E-04 3.6E-04 6