Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 18
rs8082812 0.851 0.120 18 8522684 intergenic variant C/A snv 4.6E-02 16
rs114821210 1.000 0.040 5 166089843 intergenic variant C/A snv 6.0E-03 3
rs74864598
C8orf37-AS1
1.000 0.040 8 95439207 intron variant C/A snv 4.4E-02 3
rs78314028
CYTH3
1.000 0.040 7 6163445 3 prime UTR variant C/A snv 2.2E-02 3
rs397507549
PTPN11
0.742 0.240 12 112489104 missense variant C/A;G snv 13
rs12362161 1.000 0.040 11 98834502 intergenic variant C/A;G snv 3
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs760762
PLCG1
0.851 0.120 20 41147406 intron variant C/A;T snv 0.59 16
rs2549513
MAF
0.851 0.080 16 79516830 downstream gene variant C/A;T snv 4
rs189919070
MIR4788
1.000 0.040 3 134436825 upstream gene variant C/A;T snv 3
rs7965830
LOC105369844
1.000 0.040 12 75962050 intron variant C/A;T snv 3
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs1799895
SOD3
0.683 0.360 4 24800212 missense variant C/G snv 2.3E-02 1.2E-02 26
rs8179090
TIMP2
0.752 0.280 17 78925807 upstream gene variant C/G snv 1.6E-02 12
rs10501920
CNTN5
0.882 0.080 11 99622442 intron variant C/G snv 0.14 3
rs1303946678
CYP2D6 ; NDUFA6-DT
0.925 0.040 22 42126851 missense variant C/G snv 3
rs149447933
LOC101928331 ; LOC105374942
1.000 0.040 6 14453908 intron variant C/G snv 4.4E-03 3
rs911119
CST3
0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs397516089
MYH7
0.827 0.080 14 23429807 missense variant C/G;T snv 6
rs79661299 1.000 0.040 6 42088268 downstream gene variant C/G;T snv 3