Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9912300
ACLY
0.827 0.120 17 41869011 intron variant G/A;C;T snv 4.2E-06; 0.78 5
rs1682111
ACYP2
0.742 0.240 2 54200842 intron variant A/T snv 0.56 13
rs11896604
ACYP2
0.776 0.200 2 54252062 intron variant C/A;G;T snv 8
rs843720
ACYP2 ; LOC105374610
0.752 0.280 2 54283523 intron variant T/G snv 0.52 10
rs2241766
ADIPOQ ; ADIPOQ-AS1
0.608 0.720 3 186853103 synonymous variant T/C;G snv 8.0E-06; 0.13 48
rs1042711
ADRB2
0.827 0.120 5 148826785 5 prime UTR variant C/A;G;T snv 4.2E-06; 0.68 5
rs4513061
AGBL1
0.807 0.080 15 86428401 intron variant G/A;T snv 6
rs2070600
AGER
0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs595961
AGO1
0.807 0.160 1 35902179 intron variant A/G snv 0.30 0.37 6
rs2066853
AHR
0.653 0.600 7 17339486 missense variant G/A snv 0.15 0.22 34
rs2158041
AHR
0.807 0.160 7 17328796 intron variant T/C snv 0.81 6
rs7811989
AHR
0.882 0.080 7 17331739 intron variant A/G snv 0.76 3
rs4957014
AHRR ; PDCD6
0.752 0.160 5 287899 intron variant T/G snv 0.74 11
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs778561687
AKT2
0.851 0.080 19 40235953 missense variant C/A;T snv 4.0E-06; 4.0E-06 4
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs1057519697
ALK
0.776 0.120 2 29220830 missense variant A/C snv 12
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
rs1654701
ANGPT1
0.882 0.080 8 107366717 intron variant G/A snv 0.52 3
rs4262299
ANGPT1
0.882 0.080 8 107330035 intron variant A/C;T snv 3
rs11137037
ANGPT2 ; MCPH1
0.851 0.200 8 6538661 intron variant A/C snv 0.40 4
rs11020802
ANKRD49 ; MRE11
0.882 0.080 11 94493959 upstream gene variant C/A;G;T snv 3
rs776197565
APC
0.827 0.120 5 112819214 missense variant G/C;T snv 4.0E-06; 4.0E-06 5
rs1060503291
APC
0.882 0.080 5 112835135 missense variant C/T snv 3