Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2162679
IGF1
0.851 0.240 12 102477481 intron variant C/G;T snv 6
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
rs699473
SOD3
0.827 0.160 4 24795181 intron variant C/T snv 0.54 5
rs1050283
OLR1
0.882 0.160 12 10159690 3 prime UTR variant G/A snv 0.40 4
rs12342
ADIPOR2
0.851 0.240 12 1787714 3 prime UTR variant C/A;T snv 4
rs1537378
CDKN2B-AS1
0.882 0.160 9 22061615 intron variant A/G snv 0.73 4
rs3754701
RAMP1
0.882 0.120 2 237858561 upstream gene variant A/C;T snv 4
rs4073259
ALOX5AP
0.882 0.160 13 30732134 intron variant G/A snv 0.49 4
rs7291467
LGALS2
0.851 0.160 22 37576621 intron variant G/A snv 0.49 4
rs7590387 0.882 0.120 2 237913557 downstream gene variant G/A;C snv 3
rs10304
SMTN ; SELENOM
0.925 0.120 22 31104550 3 prime UTR variant G/A snv 0.12 2
rs10898909
P2RY2
0.925 0.120 11 73241451 non coding transcript exon variant G/A snv 0.21 2
rs2072592
IGF1 ; LINC02456
0.925 0.120 12 102419854 intron variant C/T snv 2.8E-02 2
rs2238634
TBXA2R
0.925 0.200 19 3604731 intron variant A/C;T snv 2
rs2278986
SCARB1
0.925 0.120 12 124814823 intron variant A/G snv 0.28 2
rs3731245
CDKN2A
0.925 0.120 9 21972446 intron variant C/T snv 6.6E-03 2
rs3769048
RAMP1
0.925 0.120 2 237861218 intron variant G/A snv 2.2E-02 2
rs4147064
ALOX5AP
1.000 0.120 13 30745981 intron variant T/C snv 0.50 2
rs710968
LIMK1
0.925 0.120 7 74083398 intron variant A/G snv 0.75 2
rs768963
CACTIN
0.925 0.120 19 3615409 non coding transcript exon variant G/A;C snv 2
rs7956547
IGF1
0.925 0.120 12 102465038 intron variant T/C snv 0.25 2
rs978458
IGF1 ; LINC02456
0.925 0.120 12 102408461 intron variant T/C snv 0.69 2
rs10780199
CACNA1B
1.000 0.120 9 138058845 intron variant G/A snv 0.36 1
rs11137351
CACNA1B ; LOC101928786
1.000 0.120 9 138045676 intron variant C/G snv 0.23 1