Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs738490
MOV10L1
1.000 0.040 22 50092222 intron variant G/A snv 0.18 0.14 1
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 88
rs72943235 1.000 0.040 2 88201127 intergenic variant G/A snv 9.0E-02 1
rs72613567
HSD17B13
0.742 0.320 4 87310240 splice donor variant -/A delins 0.22 14
rs72563732
ADIPOQ-AS1 ; ADIPOQ
0.882 0.040 3 186854563 synonymous variant C/T snv 6.4E-05 2.6E-04 3
rs71413689 1.000 0.040 2 150398953 intergenic variant G/A snv 1.7E-02 1
rs6993
GOT2
0.925 0.080 16 58707463 3 prime UTR variant A/G snv 0.59 3
rs698718 1.000 0.040 16 68526282 upstream gene variant A/C;G;T snv 1
rs6982502 0.882 0.080 8 125467120 intron variant C/T snv 0.62 6
rs694539
NNMT
0.776 0.200 11 114262697 intron variant C/T snv 0.21 10
rs6850524
CLOCK
0.925 0.080 4 55515830 intron variant C/G;T snv 3
rs6843722
CLOCK
1.000 0.040 4 55465165 intron variant A/C snv 0.30 1
rs6834314 0.807 0.160 4 87292656 intergenic variant A/G snv 0.24 10
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs6700896
LEPR
0.827 0.160 1 65624099 intron variant C/T snv 0.44 9
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs659366
UCP2
0.724 0.520 11 73983709 non coding transcript exon variant C/T snv 0.40 17
rs6591182
EHBP1L1
0.925 0.080 11 65582285 missense variant T/G snv 0.47 0.45 2
rs6503695
STAT3
0.925 0.040 17 42347515 intron variant T/C snv 0.33 2
rs6499186 1.000 0.040 16 68626662 downstream gene variant C/T snv 0.84 1
rs6487679 0.925 0.080 12 9218736 intergenic variant C/T snv 0.80 2
rs643608 0.925 0.080 21 43348682 intergenic variant C/T snv 0.69 2
rs641738
LOC112268246 ; TMC4 ; MBOAT7
0.689 0.320 19 54173068 missense variant T/A;C;G snv 22
rs626283
TMC4 ; MBOAT7 ; LOC112268246
0.827 0.160 19 54173307 upstream gene variant C/G snv 0.61 7
rs62141163 1.000 0.040 2 31440248 regulatory region variant G/A snv 7.6E-02 2