Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3856806
PPARG
0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs3818361
CR1
0.851 0.080 1 207611623 intron variant A/G snv 0.74 6
rs3816873
MTTP
0.790 0.200 4 99583507 missense variant T/C snv 0.25 0.26 9
rs3813929
HTR2C
0.851 0.240 X 114584047 upstream gene variant C/G;T snv 5
rs3731201
CDKN2A
1.000 0.080 9 21988897 intron variant C/T snv 0.86 2
rs33954001
LOC105373000 ; SLC5A1
1.000 0.120 22 32110063 missense variant C/G;T snv 4.8E-02; 2.4E-05 2
rs2920502
PPARG
0.851 0.160 3 12287696 intron variant G/C snv 0.27 6
rs28936379
PSEN2
0.807 0.120 1 226888977 missense variant A/C;G;T snv 4.0E-06 10
rs2721068
FOXO1
0.882 0.160 13 40565575 intron variant T/C snv 0.38 4
rs2297627
FOXO1
0.925 0.120 13 40659794 intron variant A/G snv 0.41 3
rs2293855
MTMR9
0.851 0.120 8 11319901 non coding transcript exon variant G/A snv 0.35 5
rs2278426
ANGPTL8 ; DOCK6
1.000 0.080 19 11239812 missense variant C/T snv 0.11 0.11 11
rs2233580
PAX4
0.882 0.080 7 127613496 missense variant C/T snv 8.2E-03 2.1E-03 5
rs2073162
TNMD
1.000 0.080 X 100594020 synonymous variant G/A snv 0.40 0.39 2
rs199474657
TRNL1 ; ND1 ; ND2
0.752 0.360 MT 3243 non coding transcript exon variant A/G snv 15
rs1884614
LOC105372629
0.882 0.080 20 44351879 non coding transcript exon variant C/T snv 0.18 5
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1805097
IRS2
0.689 0.360 13 109782884 missense variant C/G;T snv 0.35 22
rs1805094
LEPR
0.716 0.440 1 65610269 missense variant G/C;T snv 0.16; 4.0E-06 16
rs1801483
GCGR
0.851 0.160 17 81809839 missense variant G/A snv 7.4E-03 6.3E-03 7
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1801278
IRS1
0.637 0.560 2 226795828 missense variant C/G;T snv 4.0E-06; 5.2E-02 38
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs1799999
PPP1R3A
0.882 0.160 7 113878379 missense variant C/A snv 0.22 0.17 4