Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1043307
PSMD9
0.776 0.360 12 121915890 missense variant A/C;G snv 14
rs3751143
P2RX7 ; LOC105370032
0.742 0.480 12 121184501 missense variant A/C;G snv 0.19; 4.0E-06 12
rs4923461
BDNF-AS ; LINC00678
0.925 0.120 11 27635363 intron variant A/C;G snv 5
rs17817288
FTO
1.000 0.080 16 53773852 intron variant A/C;G snv 3
rs235326
ITGB2
0.925 0.200 21 44891898 synonymous variant A/C;G snv 0.68 2
rs3752482
CPNE5
0.925 0.160 6 36765293 intron variant A/C;G snv 4.0E-06; 0.12 2
rs9894946
TP53
0.925 0.160 17 7667762 intron variant A/C;G snv 2
rs121913559
MC4R
1.000 0.080 18 60372045 missense variant A/C;G snv 4.0E-06 1
rs4784323
FTO
1.000 0.080 16 53763653 intron variant A/C;G snv 0.74 1
rs9923451
WWOX
1.000 0.080 16 78918542 intron variant A/C;G snv 1
rs854560
PON1
0.513 0.800 7 95316772 missense variant A/C;G;N;T snv 0.29 113
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs11084753 1.000 0.080 19 33831232 intergenic variant A/C;G;T snv 0.65 6
rs33980857
HBB
0.827 0.280 11 5227101 5 prime UTR variant A/C;G;T snv 5
rs3923113 0.882 0.120 2 164645339 intergenic variant A/C;G;T snv 3
rs16892496
TRHR
1.000 0.080 8 109097622 intron variant A/C;G;T snv 2
rs335170
PRDM6
0.925 0.120 5 123146549 intron variant A/C;G;T snv 2
rs7678287
SLC2A9 ; LOC105374476
1.000 0.080 4 9998877 intron variant A/C;G;T snv 2
rs2032582
ABCB1
0.538 0.800 7 87531302 missense variant A/C;T snv 0.54; 3.8E-02 97
rs7041
GC
0.576 0.800 4 71752617 missense variant A/C;T snv 0.52; 4.0E-06 64
rs2228145
IL6R
0.602 0.720 1 154454494 missense variant A/C;T snv 0.38; 1.2E-05 57
rs1271572
ESR2
0.708 0.400 14 64295199 intron variant A/C;T snv 16
rs2237895
KCNQ1
0.790 0.240 11 2835964 intron variant A/C;T snv 10
rs11152213 1.000 0.080 18 60185715 intergenic variant A/C;T snv 4
rs12463617 1.000 0.080 2 629244 regulatory region variant A/C;T snv 4