Disease: Calcification of coronary artery
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs73169578 1.000 0.080 13 21120420 intergenic variant G/A snv 3.1E-02 2
rs74155456 1.000 0.080 10 61070020 intergenic variant T/C snv 2.3E-02 2
rs7442201
NSG1
1.000 0.080 4 4360022 intron variant A/C;G snv 2
rs74570061
ARL9
1.000 0.080 4 56517605 intron variant T/C snv 3.9E-02 2
rs74910095 1.000 0.080 5 63545132 intergenic variant T/A snv 3.7E-02 2
rs75629841
MTSS1
1.000 0.080 8 124714135 intron variant G/A;T snv 2
rs76294234 1.000 0.080 4 83241025 intron variant A/G snv 1.5E-02 2
rs7689240 1.000 0.080 4 35313869 intergenic variant A/G snv 0.21 2
rs77757620
STARD9
1.000 0.080 15 42661399 intron variant C/T snv 3.8E-02 2
rs77934287 1.000 0.080 12 23071319 intron variant A/G;T snv 2
rs7804216
ACTR3C
1.000 0.080 7 149941248 intergenic variant C/G snv 0.24 2
rs8134546
LINC01426
1.000 0.080 21 34782568 intron variant T/C snv 8.7E-02 2
rs91
LOC107986777
1.000 0.080 7 24409992 intron variant T/C snv 0.41 2
rs9384331
LOC105378054
1.000 0.080 6 150279905 intergenic variant T/C snv 0.12 2
rs9641609 1.000 0.080 7 118657790 regulatory region variant A/G snv 0.38 2
rs9973676
GPR55
1.000 0.080 2 230954091 intron variant G/A snv 5.8E-02 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55