Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 17
rs2925979
CMIP
1.000 0.080 16 81501185 intron variant T/A;C snv 10
rs2145272 20 6645571 intergenic variant G/A;T snv 8
rs13130484 1.000 0.080 4 45173674 intergenic variant C/A;T snv 7
rs9930333
FTO
0.882 0.120 16 53766065 intron variant T/C;G snv 7
rs615672
HLA-DRB1
0.851 0.240 6 32606394 intergenic variant G/A;C snv 6
rs1884897 20 6632185 regulatory region variant A/G;T snv 5
rs1046934
TSEN15
1.000 0.080 1 184054395 missense variant A/C;G;T snv 0.34; 4.0E-06 4
rs10842707 12 26318431 intron variant C/G;T snv 4
rs1443512 12 53948900 downstream gene variant A/C;T snv 4
rs17819328 3 12447843 intergenic variant T/A;G snv 4
rs2033529
TDRG1
6 40380914 intron variant A/C;G snv 4
rs2820436
LYPLAL1-AS1
0.882 0.040 1 219467338 intergenic variant A/C;G snv 4
rs4715210 6 50929538 regulatory region variant C/G;T snv 4
rs7162542
ADAMTSL3
15 83845538 intron variant C/A;G;T snv 4
rs757608 17 61419916 regulatory region variant A/G;T snv 4
rs9435732
MFAP2
1 16981663 intron variant C/G;T snv 4
rs11897119
MEIS1
2 66544868 intron variant T/A;C snv 3
rs2764261
FOXO3
6 108606639 intron variant A/G;T snv 3
rs3764419
ATAD5
17 30837005 intron variant C/A;G snv 3
rs3936510
C5orf67
1.000 0.040 5 56565039 intron variant G/A;T snv 3
rs4765219
CCDC92
12 123955563 intron variant C/A;T snv 3
rs4800452
CABLES1
18 23147647 intron variant C/G;T snv 3