Disease: Hypercholesterolemia
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs693
APOB
0.708 0.440 2 21009323 synonymous variant G/A snv 0.39 0.38 24
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs3761740
HMGCR
0.882 0.160 5 75336308 intron variant C/A snv 8.2E-02 4