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
rs2231142
ABCG2
0.583 0.680 4 88131171 missense variant G/C;T snv 4.0E-06; 0.12 56
rs1154454
ADH7
0.925 0.120 4 99417185 intron variant A/G snv 0.22 2
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs182052
ADIPOQ
0.701 0.440 3 186842993 intron variant G/A snv 0.38 19
rs3774262
ADIPOQ ; ADIPOQ-AS1
0.851 0.200 3 186854025 intron variant G/A snv 0.10 5
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
rs1048798213
APC
1.000 0.120 5 112837872 missense variant C/G snv 1
rs1442780982
APC
1.000 0.120 5 112837977 missense variant C/A;G;T snv 4.0E-06 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
rs12553173
ARHGEF39 ; CA9
1.000 0.120 9 35674104 synonymous variant T/C snv 0.14 0.20 1
rs2606736
ATG7
1.000 0.120 3 11358775 intron variant C/A;T snv 4
rs6442260
ATG7
0.925 0.160 3 11549277 intron variant G/A snv 0.42 2
rs611646
ATM
0.882 0.120 11 108306370 intron variant T/A;C snv 3
rs750597831
ATM
1.000 0.120 11 108229230 missense variant C/T snv 8.0E-06 7.0E-06 2
rs587782274
ATM ; C11orf65
1.000 0.120 11 108312465 missense variant A/C snv 1