Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12567209 0.807 0.080 1 162066689 upstream gene variant G/A snv 8.6E-02 6
rs28714259 0.882 0.120 15 23463380 intergenic variant G/A snv 0.19 5
rs10189761 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 4
rs499818 0.851 0.080 6 13332235 upstream gene variant G/A snv 0.21 4
rs9351814 0.882 0.040 6 71484004 intergenic variant A/C snv 0.35 4
rs9885413 0.925 0.040 5 110840429 intergenic variant G/T snv 0.19 2
rs8187710
ABCC2
0.827 0.200 10 99851537 missense variant G/A snv 5.3E-02 8.5E-02 6
rs141322087
ABCC8
0.851 0.160 11 17404552 missense variant C/T snv 1.2E-05 2.1E-05 13
rs1344172059
ABCC8
0.882 0.080 11 17430838 missense variant C/T snv 7.0E-06 12
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
rs1815739
ACTN3
0.763 0.240 11 66560624 stop gained C/T snv 0.37 17
rs452159
ADA
1.000 0.040 20 44642461 intron variant G/T snv 0.28 2
rs1544223
ADORA3 ; TMIGD3
1.000 0.040 1 111503935 intron variant C/T snv 0.72 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
rs37369
AGXT2
0.807 0.120 5 35037010 missense variant C/T snv 0.21 0.25 9
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116