Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs9308762
INSIG2
0.925 0.120 2 118106298 intron variant C/A;G;T snv 2
rs1953124 1.000 0.040 13 65771915 regulatory region variant C/A;G;T snv 1
rs2228603
NCAN
0.790 0.360 19 19219115 missense variant C/A;T snv 2.8E-05; 5.9E-02 12
rs13306741
RAI1 ; SREBF1
1.000 0.040 17 17811708 3 prime UTR variant C/A;T snv 4.3E-03; 7.4E-06 1
rs497408 1.000 0.040 6 23993395 regulatory region variant C/A;T snv 1
rs1800795
IL6-AS1 ; IL6 ; STEAP1B
0.494 0.840 7 22727026 intron variant C/G snv 0.71 140
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
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs1800206
PPARA
0.641 0.640 22 46218377 missense variant C/G snv 4.3E-02 4.2E-02 35
rs328
LPL
0.732 0.440 8 19962213 stop gained C/G snv 9.2E-02 9.0E-02 19
rs10865710
PPARG
0.763 0.360 3 12311699 intron variant C/G snv 0.25 13
rs626283
TMC4 ; MBOAT7 ; LOC112268246
0.827 0.160 19 54173307 upstream gene variant C/G snv 0.61 7
rs1554483
CLOCK
0.882 0.160 4 55455650 intron variant C/G snv 0.33 5
rs499765 0.925 0.160 19 48763133 downstream gene variant C/G snv 0.45 2
rs1858999
GATAD2A
1.000 0.040 19 19386860 intron variant C/G snv 0.56 1
rs222054 1.000 0.040 4 71738582 downstream gene variant C/G snv 0.27 1
rs3806622
HESX1 ; APPL1
1.000 0.040 3 57226802 intron variant C/G snv 0.47 1
rs768007422
ARHGEF7
1.000 0.040 13 111277667 missense variant C/G snv 1
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs2294915
PNPLA3
1.000 0.040 22 43945024 intron variant C/G;T snv 5
rs6850524
CLOCK
0.925 0.080 4 55515830 intron variant C/G;T snv 3
rs343064 0.925 0.080 7 35515178 upstream gene variant C/G;T snv 2
rs117542855 1.000 0.040 11 1635713 regulatory region variant C/G;T snv 3.1E-02 1