Disease: Calcification of coronary artery
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs6506897 1.000 0.080 18 31215320 intergenic variant G/A snv 0.62 2
rs6506900
LOC105372049
1.000 0.080 18 31226433 intergenic variant A/C;G snv 2
rs448792
FRY
1.000 0.080 13 32103287 intron variant T/A;C snv 2
rs543554
FRY
1.000 0.080 13 32127501 intron variant A/G;T snv 2
rs8134546
LINC01426
1.000 0.080 21 34782568 intron variant T/C snv 8.7E-02 2
rs7689240 1.000 0.080 4 35313869 intergenic variant A/G snv 0.21 2
rs115689251
LOC107985068
1.000 0.080 17 36032377 intergenic variant A/C snv 1.0E-02 2
rs77757620
STARD9
1.000 0.080 15 42661399 intron variant C/T snv 3.8E-02 2
rs7442201
NSG1
1.000 0.080 4 4360022 intron variant A/C;G snv 2
rs12040333
ST3GAL3
1.000 0.080 1 43848369 intron variant G/A;C snv 2
rs74570061
ARL9
1.000 0.080 4 56517605 intron variant T/C snv 3.9E-02 2
rs74155456 1.000 0.080 10 61070020 intergenic variant T/C snv 2.3E-02 2
rs74910095 1.000 0.080 5 63545132 intergenic variant T/A snv 3.7E-02 2
rs1481805 1.000 0.080 8 71121190 intron variant A/T snv 0.58 2
rs113805659
MAGI2
1.000 0.080 7 78663475 intron variant G/C snv 6.1E-02 2
rs76294234 1.000 0.080 4 83241025 intron variant A/G snv 1.5E-02 2