Disease: Serum total cholesterol measurement
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 41
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs12579302
ATP2B1
0.851 0.120 12 89656726 intron variant A/G snv 0.15 19
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 18
rs1378942
CSK
0.790 0.240 15 74785026 intron variant C/A;T snv 16
rs740746 10 114033028 intergenic variant G/A snv 0.70 8
rs17030613
CAPZA1
1 112648185 intron variant A/C snv 0.19 7