Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs132793 0.851 0.160 22 41667677 downstream gene variant A/C;G;T snv 7
rs7859384 0.882 0.120 9 79507370 intron variant A/C;G snv 6
rs11813268 0.925 0.120 10 103922538 upstream gene variant C/T snv 0.31 2
rs1417080 0.925 0.120 9 79515946 non coding transcript exon variant T/C snv 0.35 2
rs3118523 0.925 0.120 9 134443675 downstream gene variant G/A snv 0.75 2
rs6466135 0.925 0.120 7 106861053 upstream gene variant A/G snv 0.71 2
rs7132434 0.925 0.120 12 26319629 non coding transcript exon variant A/G snv 0.62 2
rs748964 0.925 0.120 9 134442243 downstream gene variant C/G;T snv 2
rs11263654 1.000 0.120 11 69423355 upstream gene variant C/T snv 0.11 1
rs13376700 1.000 0.120 1 51011971 intergenic variant T/A snv 0.48 1
rs7765284 1.000 0.120 6 85068104 intergenic variant C/A snv 0.13 1
rs78971134 1.000 0.120 12 107258753 intergenic variant A/G snv 7.7E-02 1
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs6713088
ACYP2
0.763 0.200 2 54118332 intron variant C/G snv 0.48 9
rs843711
ACYP2
0.790 0.200 2 54251980 intron variant C/T snv 0.41 7
rs1154454
ADH7
0.925 0.120 4 99417185 intron variant A/G snv 0.22 2
rs182052
ADIPOQ
0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs3889728
AGT
1.000 0.120 1 230713085 intron variant C/T snv 0.24 2
rs5186
AGTR1
0.630 0.560 3 148742201 3 prime UTR variant A/C snv 0.23 0.21 38
rs1492078
AGTR1
1.000 0.120 3 148697390 upstream gene variant T/C snv 0.50 1
rs1800435
ALAD
0.827 0.200 9 113391611 missense variant C/G snv 8.3E-02 6.1E-02 7
rs2761016
ALAD
0.925 0.120 9 113391072 intron variant T/C snv 0.59 2
rs7913447
ANAPC16
1.000 0.120 10 72232282 intron variant C/A;T snv 1
rs1130409
APEX1
0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs405509
APOE
0.667 0.480 19 44905579 upstream gene variant T/G snv 0.58 30