Disease: Cardiovascular Diseases
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs58542926
TM6SF2
0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs1044498
ENPP1
0.752 0.360 6 131851228 missense variant A/C;G snv 0.19 15
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs2241883
FABP1
0.763 0.360 2 88124547 missense variant T/C snv 0.30 0.29 14
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs1800777
CETP
0.724 0.280 16 56983407 missense variant G/A snv 3.7E-02 2.8E-02 17
rs17321515 0.776 0.200 8 125474167 intron variant A/G snv 0.49 16
rs694539
NNMT
0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs5182
AGTR1
0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10