Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs662799
APOA5
0.689 0.480 11 116792991 upstream gene variant G/A snv 0.90 33
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs579459 0.752 0.320 9 133278724 upstream gene variant C/T snv 0.81 28
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 27
rs657152
ABO
0.882 0.200 9 133263862 intron variant A/C;T snv 22
rs12075
CADM3-AS1 ; ACKR1
0.724 0.240 1 159205564 missense variant G/A snv 0.51 0.66 22
rs1121980
FTO
0.807 0.240 16 53775335 intron variant G/A;C snv 18
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 17
rs8040868
CHRNA3
0.742 0.240 15 78618839 synonymous variant T/C snv 0.35 0.37 17
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs687289
ABO
1.000 0.120 9 133261703 intron variant A/G snv 15
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 10
rs507666
ABO
1.000 0.040 9 133273983 intron variant A/G snv 8
rs1443438
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv 8
rs8176719
ABO
0.925 0.120 9 133257521 frameshift variant -/C ins 0.37 0.35 6
rs2228468
ACKR2 ; KRBOX1 ; CYP8B1
0.882 0.120 3 42865620 missense variant A/C;T snv 0.43; 8.3E-03 6
rs7193144
FTO
0.925 0.120 16 53776774 intron variant T/C snv 0.40 6
rs7850258
PTCSC2
0.827 0.200 9 97786731 intron variant A/G snv 0.72 6
rs925489
PTCSC2
0.882 0.080 9 97784318 intron variant C/T snv 0.71 6
rs2427837
FCER1A
0.851 0.160 1 159288755 upstream gene variant G/A snv 0.20 5
rs9926289
FTO
0.882 0.160 16 53786591 intron variant G/A snv 0.41 5
rs3733402
KLKB1
1.000 0.040 4 186236880 missense variant G/A;C snv 0.54 5
rs3741298
ZPR1
11 116786845 intron variant C/T snv 0.73 5