Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs2107595 0.732 0.280 7 19009765 regulatory region variant G/A snv 0.19 15
rs8075977 0.827 0.160 17 1757507 upstream gene variant T/C snv 0.37 5
rs2768759 0.851 0.200 1 156882671 downstream gene variant A/C;G snv 4
rs3092952 0.925 0.160 X 136644791 upstream gene variant A/G snv 0.29 3
rs3092920 0.925 0.160 X 136661832 downstream gene variant G/T snv 0.23 2
rs6141803 1.000 0.120 20 32752550 TF binding site variant T/C snv 0.13 2
rs1239681664
ABCA1
0.716 0.320 9 104818690 synonymous variant A/G snv 7.0E-06 15
rs559110055
ABCA1
0.925 0.160 9 104840491 missense variant A/G snv 4.0E-06 2
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs676457
ABO
1.000 0.120 9 133270797 intron variant T/A snv 3
rs1267969615
ACE
0.532 0.760 17 63490960 missense variant T/C snv 4.0E-06 100
rs4343
ACE
0.742 0.480 17 63488670 synonymous variant G/A snv 0.53 14
rs1994016
ADAMTS7
0.851 0.160 15 78787892 intron variant C/T snv 0.30 7
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
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
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs2029253
ALOX5
0.925 0.200 10 45396036 intron variant A/G snv 0.37 3
rs10507391
ALOX5AP
0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs4769874
ALOX5AP
0.827 0.240 13 30752304 intron variant G/A snv 5.8E-02 5
rs9508835
ALOX5AP
1.000 0.120 13 30760561 intron variant C/A snv 0.23 1