Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs11833579 0.827 0.200 12 666033 upstream gene variant G/A snv 0.25 6
rs7590387 0.882 0.120 2 237913557 downstream gene variant G/A;C snv 3
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs2066715
ABCA1
0.807 0.160 9 104825752 missense variant C/T snv 8.2E-02 5.5E-02 7
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs12342
ADIPOR2
0.851 0.240 12 1787714 3 prime UTR variant C/A;T snv 4
rs4918
AHSG
0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 12
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs10507391
ALOX5AP
0.776 0.320 13 30737959 intron variant A/T snv 0.52 10
rs9551963
ALOX5AP
0.851 0.160 13 30758410 intron variant A/C;T snv 6
rs9579646
ALOX5AP
0.851 0.160 13 30736442 intron variant G/A;T snv 6
rs4073259
ALOX5AP
0.882 0.160 13 30732134 intron variant G/A snv 0.49 4
rs4147064
ALOX5AP
1.000 0.120 13 30745981 intron variant T/C snv 0.50 2
rs4769055
ALOX5AP
1.000 0.120 13 30735693 intron variant C/A snv 0.41 0.47 1
rs755403632
BMS1
1.000 0.120 10 42792991 missense variant C/G;T snv 4.0E-06; 4.0E-06 1
rs4919862
BSG
1.000 0.120 19 582253 intron variant T/C snv 0.82 1
rs10780199
CACNA1B
1.000 0.120 9 138058845 intron variant G/A snv 0.36 1
rs7042521
CACNA1B ; LOC100133077
1.000 0.120 9 137889440 intron variant C/G snv 0.31 1
rs11137351
CACNA1B ; LOC101928786
1.000 0.120 9 138045676 intron variant C/G snv 0.23 1
rs768963
CACTIN
0.925 0.120 19 3615409 non coding transcript exon variant G/A;C snv 2
rs2271875
CACTIN
1.000 0.120 19 3626924 upstream gene variant T/C snv 0.68 1
rs3731245
CDKN2A
0.925 0.120 9 21972446 intron variant C/T snv 6.6E-03 2
rs2383207
CDKN2B-AS1
0.695 0.280 9 22115960 intron variant A/G snv 0.64 22
rs1537378
CDKN2B-AS1
0.882 0.160 9 22061615 intron variant A/G snv 0.73 4