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
rs10978777 1.000 0.080 9 107268309 intergenic variant G/A;C snv 2
rs113533135
LRP1B
1.000 0.080 2 140268867 intron variant T/C snv 2.0E-02 2
rs113805659
MAGI2
1.000 0.080 7 78663475 intron variant G/C snv 6.1E-02 2
rs114031744 1.000 0.080 10 123610085 intergenic variant A/G snv 1.7E-02 2
rs11509197 1.000 0.080 7 118641356 intergenic variant C/T snv 0.38 2
rs115689251
LOC107985068
1.000 0.080 17 36032377 intergenic variant A/C snv 1.0E-02 2
rs117854110 1.000 0.080 7 105603002 upstream gene variant C/A;T snv 2
rs12040333
ST3GAL3
1.000 0.080 1 43848369 intron variant G/A;C snv 2
rs13175840 1.000 0.080 5 133861647 regulatory region variant A/G snv 0.25 2
rs1481805 1.000 0.080 8 71121190 intron variant A/T snv 0.58 2
rs1532002
LRP1B
1.000 0.080 2 140292500 intron variant G/A snv 2.3E-02 2
rs16879003
ATXN1
1.000 0.080 6 16745008 intron variant T/C;G snv 2
rs17214144
OSBPL3
1.000 0.080 7 24846128 intron variant T/C snv 0.20 2
rs2680830
VSNL1
1.000 0.080 2 17596817 intron variant A/G;T snv 0.94 2
rs4272321
PTPRN2
1.000 0.080 7 158159143 intron variant A/G snv 4.6E-04 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
rs59490629
PDSS2
1.000 0.080 6 107256268 intron variant G/A snv 8.5E-02 2
rs59811240
MTSS1
1.000 0.080 8 124709787 intron variant C/A snv 1.3E-02 2
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
rs6606859
GABRG3
1.000 0.080 15 27032254 intron variant C/A;T snv 2
rs6754498
LOC107985783
1.000 0.080 2 185953121 non coding transcript exon variant A/C;G;T snv 2
rs6898559
ALDH7A1
1.000 0.080 5 126557237 intron variant G/A snv 0.66 2