Disease: High density lipoprotein measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 92
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 34
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 21
rs2954021 1.000 0.040 8 125469835 intron variant A/G snv 0.54 15
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7
rs13135092
SLC39A8
4 102276925 intron variant A/G snv 5.1E-02 4
rs72836561
CD300LG
17 43848758 missense variant C/T snv 2.2E-02 2.0E-02 4
rs4805881
PEPD
19 33405526 intron variant A/C snv 0.69 3
rs2494748
AKT1
14 104792555 intron variant C/T snv 0.51 0.48 2