Disease: High density lipoprotein measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3832016
CELSR2
1 109275536 3 prime UTR variant -/T ins 0.74 4
rs2980875 8 125469505 intron variant A/C;G;T snv 6
rs12394306
SYN1
X 47576648 splice region variant A/C;T snv 4.3E-03 4
rs6657811
CELSR2
1 109264661 intron variant A/C;T snv 4.0E-06; 0.10 4
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 17
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 24
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs1874148
VCL
10 74114657 intron variant A/G snv 1.8E-02 6
rs2001844 0.882 0.040 8 125466503 upstream gene variant A/G snv 0.43 9
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs2303790
CETP
0.724 0.280 16 56983380 missense variant A/G snv 2.6E-03 6.5E-04 19
rs2678379
APOB
1.000 0.080 2 21003688 intron variant A/G snv 0.76 8
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs33980385
CYP2B6
19 40991388 missense variant A/G snv 6
rs370911
NOS1AP
1 162323515 intron variant A/G snv 0.99 6
rs3731215
CDKN2A
9 21985772 intron variant A/G snv 1.2E-03 5
rs4251583
IRAK4
12 43783705 missense variant A/G snv 8.6E-04 1.1E-03 6
rs4253642
LOC105373074 ; PPARA
22 46167520 intron variant A/G snv 7.1E-03 5
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs675504 11 102959002 upstream gene variant A/G snv 0.98 5
rs7218945
NCOR1
17 16133280 intron variant A/G snv 2.5E-02 4
rs737410
ARRB1
11 75315038 intron variant A/G snv 4.3E-02 6