Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs1258130495
EDNRA
0.882 0.040 4 147485727 missense variant G/A snv 3
rs899115126
EDNRA
0.882 0.080 4 147542603 missense variant G/C snv 3
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
rs5744680
POLK
0.851 0.120 5 75584065 intron variant G/A snv 0.55 18
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs4704221
CERT1
0.851 0.120 5 75463358 intron variant T/A;C snv 16
rs2149954
LINC02227
0.882 0.080 5 158393594 intron variant C/T snv 0.37 5
rs991104525
ARSB
0.882 0.160 5 78969051 missense variant G/A snv 1.2E-05 7.7E-05 4
rs112434206 1.000 0.040 5 33083283 intron variant A/C;G snv 7.6E-03 3
rs114821210 1.000 0.040 5 166089843 intergenic variant C/A snv 6.0E-03 3
rs1700575
LOC105374647
1.000 0.040 5 8543925 intron variant A/T snv 0.26 3
rs541284506 1.000 0.040 5 30425422 intergenic variant G/A snv 4.4E-03 3
rs2241562
HRH2
0.925 0.040 5 175684809 intron variant G/C;T snv 1.0E-03 2
rs9885413 0.925 0.040 5 110840429 intergenic variant G/T snv 0.19 2
rs2275913
IL17A
0.514 0.760 6 52186235 upstream gene variant G/A snv 0.28 105
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs5370
EDN1
0.630 0.520 6 12296022 missense variant G/T snv 0.23 0.21 37
rs10455872
LPA
0.662 0.320 6 160589086 intron variant A/G snv 4.3E-02 33
rs1800624
PBX2 ; AGER
0.658 0.480 6 32184610 upstream gene variant A/G;T snv 33
rs1800730
HFE ; LOC108783645
0.649 0.480 6 26090957 missense variant A/T snv 1.0E-02 1.0E-02 32
rs3798220
LPA
0.732 0.160 6 160540105 missense variant T/C snv 5.6E-02 3.1E-02 16