Disease: Heart failure
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12310617 0.851 0.120 12 3060327 intergenic variant C/T snv 0.11 16
rs12420422 0.851 0.120 11 123009573 intergenic variant G/A snv 3.4E-02 16
rs17140821 0.851 0.120 7 19177581 regulatory region variant G/A snv 7.9E-02 16
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs2866611 0.851 0.120 20 41322165 upstream gene variant A/T snv 0.58 16
rs2980853 0.851 0.120 8 125466108 upstream gene variant A/C snv 0.43 16
rs460976 0.851 0.120 21 41463567 downstream gene variant A/G;T snv 7
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 18
rs499818 0.851 0.080 6 13332235 upstream gene variant G/A snv 0.21 4
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs799165 0.851 0.120 7 73637727 intergenic variant T/A snv 0.13 17
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs9351814 0.882 0.040 6 71484004 intergenic variant A/C snv 0.35 4
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs1799752
ACE
0.677 0.480 17 63488529 intron variant -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT delins 25
rs1042713
ADRB2
0.576 0.800 5 148826877 missense variant G/A snv 0.42 0.43 63
rs1042714
ADRB2
0.597 0.640 5 148826910 stop gained G/C;T snv 0.68 54
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38