Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs939348
THRA
0.851 0.240 17 40075600 intron variant T/C;G snv 5
rs939347
NR1D1
0.925 0.120 17 40100440 5 prime UTR variant G/A snv 0.28 2
rs9380559 1.000 0.080 6 36239821 upstream gene variant A/G snv 0.48 2
rs9380526
FKBP5
1.000 0.080 6 35690550 intron variant C/T snv 0.64 1
rs9356744
CDKAL1
0.882 0.120 6 20685255 intron variant T/C snv 0.42 7
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs9328321
FARS2
1.000 0.080 6 5600205 intron variant G/A;C snv 1
rs9308762
INSIG2
0.925 0.120 2 118106298 intron variant C/A;G;T snv 2
rs9302652
FTO
1.000 0.080 16 53832063 intron variant C/T snv 0.74 3
rs9300039 0.851 0.160 11 41893816 intergenic variant C/A snv 9.8E-02 4
rs9299
HOXB5 ; HOXB3 ; HOXB-AS3
1.000 0.080 17 48592068 3 prime UTR variant C/A;T snv 2
rs9282861
SULT1A1
0.658 0.440 16 28606193 missense variant C/T snv 31
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs925946
BDNF-AS
0.882 0.120 11 27645655 intron variant T/G snv 0.72 9
rs921971 1.000 0.080 18 60194430 upstream gene variant T/C snv 0.21 2
rs920859222
ADIPOQ-AS1 ; ADIPOQ
1.000 0.080 3 186853158 missense variant G/A snv 1.4E-05 1
rs918031
FTO
0.925 0.120 16 54084951 intron variant C/T snv 0.53 2
rs917346005
CADM2
0.925 0.080 3 85912502 missense variant A/G snv 2
rs895819
MIR23A ; LOC284454 ; MIR27A ; MIR24-2
0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs894160
PLIN1
0.882 0.120 15 89668592 intron variant C/T snv 0.29 4
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 7
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 6
rs886040857
EIF2S3
0.882 0.240 X 24076757 frameshift variant TCAA/- delins 7
rs878909905
MC4R
1.000 0.080 18 60371829 stop gained C/T snv 1
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213