Disease: CORONARY ARTERY DISEASE, AUTOSOMAL DOMINANT, 1
Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 20
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 17
rs1122608
SMARCA4
0.763 0.120 19 11052925 intron variant G/T snv 0.18 7
rs12413409
CNNM2
0.790 0.200 10 102959339 intron variant G/A snv 9.0E-02 6
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 6
rs515135 0.807 0.160 2 21063185 intergenic variant T/C snv 0.73 6
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 4
rs6725887
WDR12
0.851 0.080 2 202881162 intron variant T/C snv 8.9E-02 4
rs9982601 0.851 0.080 21 34226827 intron variant C/T snv 0.15 4
rs11556924
ZC3HC1
0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 3
rs12190287
TCF21
0.708 0.280 6 133893387 3 prime UTR variant C/G;T snv 3
rs12936587 0.882 0.080 17 17640408 regulatory region variant G/A snv 0.38 3
rs17114036
PLPP3
0.851 0.120 1 56497149 intron variant A/G snv 0.11 3
rs2895811
HHIPL1
0.851 0.080 14 99667605 intron variant T/A;C snv 3
rs4773144
COL4A1 ; COL4A2
0.827 0.080 13 110308365 intron variant A/G snv 0.42 3
rs501120 0.763 0.240 10 44258419 downstream gene variant T/C snv 0.24 3
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 3
rs9818870
MRAS
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 3