Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs34729281
SUGP2
19 19009572 intron variant -/G delins 2
rs7203984
CETP
16 56965346 intron variant A/C snv 0.31 7
rs11216126 1.000 0.040 11 116746524 downstream gene variant A/C snv 0.11 4
rs3858076
ABCA1
9 104893841 intron variant A/C snv 0.20 3
rs480392
NTNG1
1 107436774 synonymous variant A/C snv 0.99 0.95 3
rs6726798
VIL1
2 218436132 intron variant A/C snv 0.94 3
rs7000460
LPL
8 19946291 intron variant A/C snv 7.9E-02 3
rs353616
CD44
11 35155029 intron variant A/C snv 1.9E-02 2
rs643830
NCAM1
11 113235826 intron variant A/C snv 1.5E-02 2
rs6810819
NOCT
4 139015171 upstream gene variant A/C snv 3.4E-02 2
rs7222232
GAS7
17 10033485 intron variant A/C snv 1.3E-02 2
rs2943634 0.763 0.200 2 226203364 intergenic variant A/C;G snv 15
rs4660293
PABPC4
1 39562508 non coding transcript exon variant A/C;G snv 5
rs10489615
GALNT2
1 230169242 intron variant A/C;G snv 3
rs2075847
WTAPP1 ; MMP1
11 102799093 intron variant A/C;G snv 3
rs2863973
SMPD3
16 68375532 intron variant A/C;G snv 2
rs4784745
CETP
16 56980963 intron variant A/C;G snv 2
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs2652834 15 63104668 intron variant A/C;G;T snv 2
rs485671
LIPC ; ALDH1A2 ; LIPC-AS1
15 58448935 intron variant A/C;T snv 5
rs12394306
SYN1
X 47576648 splice region variant A/C;T snv 4.3E-03 4
rs486394
LINC02702
1.000 0.040 11 116655605 intron variant A/C;T snv 4
rs4986970
LCAT
0.925 0.080 16 67942417 missense variant A/C;T snv 4.0E-06; 1.7E-02 4
rs970548
MARCHF8
10 45517829 intron variant A/C;T snv 3
rs289715
CETP
16 56974596 intron variant A/C;T snv 2