Disease: Myocardial Infarction
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12762303
ALOX5
0.851 0.080 10 45373723 upstream gene variant T/C snv 0.17 4
rs12953
PECAM1
0.763 0.200 17 64356203 missense variant C/A;T snv 0.38 9
rs1310478538
C3
0.851 0.080 19 6713295 missense variant C/G snv 1.4E-05 4
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs1333045
CDKN2B-AS1
0.776 0.280 9 22119196 non coding transcript exon variant T/C snv 0.50 14
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 24
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs1412444
LIPA
0.851 0.120 10 89243170 intron variant C/T snv 0.37 4
rs1412829
CDKN2B-AS1
0.742 0.400 9 22043927 intron variant A/G snv 0.28 14
rs1433099
SPC24 ; LDLR
0.882 0.160 19 11131982 3 prime UTR variant T/A;C snv 3
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs16880442
ITGA1
0.925 0.080 5 52889863 non coding transcript exon variant G/A;T snv 2
rs17251221
CASR
0.724 0.360 3 122274400 intron variant A/G snv 0.11 18
rs17300539
ADIPOQ
0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs1746048 0.776 0.120 10 44280376 downstream gene variant C/T snv 0.25 8
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs1800469
B9D2 ; TGFB1
0.547 0.760 19 41354391 intron variant A/G snv 0.69 78
rs1800683
LOC100287329 ; LTA
0.807 0.240 6 31572294 5 prime UTR variant G/A;C snv 0.39 6
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs1801157
CXCL12
0.611 0.600 10 44372809 3 prime UTR variant C/T snv 0.16 46
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs180803
BCRP1 ; POM121L9P
0.925 0.080 22 24262890 intron variant G/A;T snv 2
rs1867624 0.851 0.080 17 64309731 upstream gene variant C/T snv 0.65 4
rs1870634 0.851 0.080 10 43985363 downstream gene variant T/G snv 0.59 4