Disease: Cardiovascular Diseases
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10838738
MTCH2
1.000 0.080 11 47641497 intron variant A/G snv 0.28 6
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1544410
VDR
0.542 0.760 12 47846052 intron variant C/A;G;T snv 78
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
rs2234693
ESR1
0.555 0.680 6 151842200 intron variant T/C snv 0.47 77
rs2237892
KCNQ1
0.790 0.320 11 2818521 intron variant C/T snv 9.2E-02 16
rs2237895
KCNQ1
0.790 0.240 11 2835964 intron variant A/C;T snv 10
rs2239179
VDR
0.790 0.200 12 47863983 intron variant T/C snv 0.39 9
rs4402960
IGF2BP2
0.724 0.400 3 185793899 intron variant G/T snv 0.38 21
rs4923461
BDNF-AS ; LINC00678
0.925 0.120 11 27635363 intron variant A/C;G snv 5
rs6731302
LINC01122
1.000 0.080 2 58606358 intron variant A/G;T snv 2
rs7069102
SIRT1
0.790 0.440 10 67903362 intron variant C/G snv 0.64 10
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 62
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs10938397 0.851 0.200 4 45180510 intergenic variant A/G snv 0.37 19
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 6
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63