Disease: Calcification of coronary artery
Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs72928364
ABI3BP
1.000 0.080 3 100894935 intron variant C/T snv 0.39 2
rs117854110 1.000 0.080 7 105603002 upstream gene variant C/A;T snv 2
rs59490629
PDSS2
1.000 0.080 6 107256268 intron variant G/A snv 8.5E-02 2
rs10978777 1.000 0.080 9 107268309 intergenic variant G/A;C snv 2
rs11509197 1.000 0.080 7 118641356 intergenic variant C/T snv 0.38 2
rs9641609 1.000 0.080 7 118657790 regulatory region variant A/G snv 0.38 2
rs114031744 1.000 0.080 10 123610085 intergenic variant A/G snv 1.7E-02 2
rs59811240
MTSS1
1.000 0.080 8 124709787 intron variant C/A snv 1.3E-02 2
rs75629841
MTSS1
1.000 0.080 8 124714135 intron variant G/A;T snv 2
rs6898559
ALDH7A1
1.000 0.080 5 126557237 intron variant G/A snv 0.66 2
rs13175840 1.000 0.080 5 133861647 regulatory region variant A/G snv 0.25 2
rs113533135
LRP1B
1.000 0.080 2 140268867 intron variant T/C snv 2.0E-02 2
rs1532002
LRP1B
1.000 0.080 2 140292500 intron variant G/A snv 2.3E-02 2
rs7804216
ACTR3C
1.000 0.080 7 149941248 intergenic variant C/G snv 0.24 2
rs9384331
LOC105378054
1.000 0.080 6 150279905 intergenic variant T/C snv 0.12 2
rs4272321
PTPRN2
1.000 0.080 7 158159143 intron variant A/G snv 4.6E-04 2
rs16879003
ATXN1
1.000 0.080 6 16745008 intron variant T/C;G snv 2
rs2680830
VSNL1
1.000 0.080 2 17596817 intron variant A/G;T snv 0.94 2
rs6754498
LOC107985783
1.000 0.080 2 185953121 non coding transcript exon variant A/C;G;T snv 2
rs73169578 1.000 0.080 13 21120420 intergenic variant G/A snv 3.1E-02 2
rs77934287 1.000 0.080 12 23071319 intron variant A/G;T snv 2
rs9973676
GPR55
1.000 0.080 2 230954091 intron variant G/A snv 5.8E-02 2
rs91
LOC107986777
1.000 0.080 7 24409992 intron variant T/C snv 0.41 2
rs17214144
OSBPL3
1.000 0.080 7 24846128 intron variant T/C snv 0.20 2
rs6606859
GABRG3
1.000 0.080 15 27032254 intron variant C/A;T snv 2