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
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 32
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1927911
TLR4
0.658 0.640 9 117707776 intron variant A/G snv 0.62 28
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs17817449
FTO
0.716 0.560 16 53779455 intron variant T/A;G snv 21
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs4925386
LAMA5
0.776 0.080 20 62345988 intron variant T/C snv 0.56 14
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins 11
rs7837328
CASC8 ; PCAT1 ; POU5F1B
0.882 0.120 8 127410882 intron variant A/G snv 0.52 8
rs2302615
ODC1-DT ; SNORA80B ; ODC1
0.807 0.120 2 10448012 intron variant C/T snv 0.31 7
rs10808555
PCAT1 ; POU5F1B ; CASC8
0.925 0.080 8 127397266 intron variant G/A snv 0.65 6
rs7131056
DRD2
0.827 0.200 11 113459052 intron variant A/C snv 0.51 6
rs10505476
PCAT1 ; POU5F1B ; CASC8
8 127395871 intron variant C/T snv 0.38 3
rs2838958
SLC19A1
1.000 0.080 21 45528653 intron variant G/A snv 0.45 3
rs17503908
ATM ; C11orf65
1.000 0.080 11 108344670 intron variant T/G snv 6.7E-02 2
rs4952490
SLC8A1-AS1 ; SLC8A1
1.000 0.080 2 40145564 intron variant A/G snv 0.33 2
rs6586714
NAT1
1.000 8 18216433 intron variant A/G snv 0.84 2
rs1201299
TBL1XR1
3 177053096 intron variant C/T snv 1.7E-02 1
rs2720574
PDGFRL
8 17578682 intron variant C/A;G;T snv 1
rs2855798
KCNJ1 ; LOC107984409
11 128863066 intron variant G/T snv 0.21 1
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 11
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs1535989 0.925 0.080 13 105370372 intergenic variant A/G;T snv 4
rs150766139
NTHL1 ; TSC2
0.742 0.320 16 2046238 stop gained G/A snv 1.4E-03 1.4E-03 13