Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs148133894 1.000 0.040 16 24584678 intergenic variant T/C snv 2.4E-03 3
rs188344082 1.000 0.040 1 18783262 intergenic variant G/A snv 1.8E-02 3
rs541284506 1.000 0.040 5 30425422 intergenic variant G/A snv 4.4E-03 3
rs61945053 1.000 0.040 13 27021678 upstream gene variant G/A snv 2.5E-02 3
rs74056623 1.000 0.040 1 18784584 intergenic variant G/A snv 8.3E-02 3
rs74056624 1.000 0.040 1 18790006 intergenic variant G/A snv 2.3E-02 3
rs79661299 1.000 0.040 6 42088268 downstream gene variant C/G;T snv 3
rs9885413 0.925 0.040 5 110840429 intergenic variant G/T snv 0.19 2
rs10519210 1.000 0.040 15 63445726 intergenic variant T/C;G snv 1
rs11172782 1.000 0.040 12 58865846 intergenic variant A/G snv 0.12 1
rs1520832 1.000 0.040 12 42859612 regulatory region variant T/C;G snv 1
rs4528684 1.000 0.040 19 14240762 intergenic variant C/T snv 0.12 1
rs548097 1.000 0.040 13 75202132 intergenic variant G/C;T snv 1
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
rs2210327
ADAMTSL1
1.000 0.040 9 18109237 intron variant A/T snv 3.4E-02 1
rs1801253
ADRB1
0.683 0.440 10 114045297 missense variant G/C snv 0.74 0.69 34
rs1801252
ADRB1
0.724 0.320 10 114044277 missense variant A/G snv 0.15 0.17 17
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
rs1800888
ADRB2
0.695 0.400 5 148827322 missense variant C/T snv 9.1E-03 9.1E-03 23
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38