Disease: Atherosclerosis
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30
rs11591147
PCSK9
0.677 0.360 1 55039974 missense variant G/A;T snv 1.2E-02 28
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 16
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 16
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs445925
APOC1
0.882 0.080 19 44912383 non coding transcript exon variant G/A;C snv 10
rs67608943
PCSK9
0.851 0.080 1 55046549 stop gained C/G;T snv 1.9E-04 8
rs28362286
PCSK9
0.851 0.080 1 55063542 stop gained C/A;T snv 5.6E-04 6