Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs146292819
ABCA1
0.790 0.240 9 104794495 missense variant T/G snv 2.9E-04 3.8E-04 9
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs4961
ADD1
0.683 0.400 4 2904980 missense variant G/A;T snv 1.2E-05; 0.20 27
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
rs5049
AGT
1.000 0.040 1 230714337 intron variant C/T snv 0.16 3
rs5182
AGTR1
0.742 0.160 3 148741608 synonymous variant C/T snv 0.49 0.41 16
rs12713559
APOB
0.776 0.120 2 21006196 missense variant G/A snv 3.4E-04 5.0E-04 10
rs144467873
APOB
0.776 0.120 2 21006289 missense variant G/A snv 1.7E-04 6.3E-05 9
rs2968915
ATP6AP2
1.000 0.040 X 40580182 intron variant G/A snv 3
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 60
rs200786329
COL4A1
0.925 13 110201467 missense variant G/A snv 5.2E-05 1.7E-04 3
rs397514624
COL4A1
0.925 13 110187254 missense variant G/A;C;T snv 1.6E-05; 4.0E-06 3
rs3742264
CPB2 ; CPB2-AS1
0.742 0.400 13 46073959 missense variant C/T snv 0.31 0.35 17
rs1926447
CPB2 ; CPB2-AS1
0.807 0.440 13 46055809 missense variant A/G snv 0.74 0.77 11
rs3732378
CX3CR1
0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 48
rs3732379
CX3CR1
0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs4673
CYBA
0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs9333025
CYP4A11
0.851 0.200 1 46931231 intron variant C/T snv 9.4E-02 8
rs9332978
CYP4A11
0.882 0.040 1 46942278 upstream gene variant T/C snv 7.3E-02 5
rs1126742
CYP4A11
0.925 0.040 1 46932824 missense variant A/G snv 0.17 0.20 4
rs2108622
CYP4F2
0.742 0.280 19 15879621 missense variant C/T snv 0.27 0.22 20
rs1558139
CYP4F2
0.851 0.160 19 15886754 intron variant G/A snv 0.46 6
rs516115
DCN
12 91163515 intron variant T/C snv 0.38 1