Disease: Cardiovascular Diseases
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs117539635
PAQR5
15 69390577 intron variant A/G snv 1.6E-02 2
rs6686889 1 24703979 upstream gene variant C/A;G;T snv 2
rs67330701
MYEOV
11 69312240 intron variant C/A;T snv 2
rs2760061 1 228003374 upstream gene variant T/A snv 0.55 3
rs3821843
CACNA1D
3 53523985 intron variant G/A snv 0.72 3
rs612652
LSP1
11 1865986 intron variant T/C snv 0.55 3
rs687914
PRKCE ; LOC102724965
2 45651621 5 prime UTR variant G/A;T snv 3
rs72656645
APOLD1 ; LOC107984129
12 12728121 intron variant A/G snv 0.21 3
rs73033340
ZFAND2A
7 1156056 intron variant A/G snv 2.7E-02 3
rs74439044
NAA38
17 7877701 intron variant T/C snv 8.9E-02 3
rs76452347
HRCT1
9 35906474 missense variant C/G;T snv 0.15 0.16 3
rs893929 4 143266227 intergenic variant G/A snv 0.42 3
rs139491786
SLC9A3R2
16 2036420 missense variant C/T snv 3.4E-03 3.5E-03 4
rs3735533
HOTTIP
7 27206274 non coding transcript exon variant T/C snv 0.93 4
rs4277405 17 63471557 upstream gene variant C/T snv 0.63 4
rs4387287
STN1
10 103918139 5 prime UTR variant A/C snv 0.69 4
rs6031431
JPH2
20 44166512 intron variant A/G snv 0.46 4
rs10059884 5 32832368 regulatory region variant C/A;T snv 5
rs12978472
INSR
19 7257979 intron variant C/G;T snv 5
rs167479
RGL3
19 11416089 missense variant T/A;C;G snv 5
rs1894400
FES
15 90885725 intron variant C/T snv 0.28 5
rs3790604
WNT2B
1 112504257 intron variant C/A snv 7.8E-02 5
rs62434109
PLEKHG1
6 150654176 intron variant T/G snv 8.4E-02 5
rs6271
DBH-AS1 ; DBH
1.000 0.040 9 133657152 missense variant C/T snv 4.6E-02 4.8E-02 5
rs7125196
LOC105369329
11 61505093 intron variant T/C snv 0.16 5