Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9922619
FTO
1.000 0.080 16 53797859 intron variant G/T snv 0.35 2
rs9922047
FTO
1.000 0.080 16 53772368 intron variant C/G snv 0.58 2
rs9921255
FTO
1.000 0.080 16 53975416 intron variant T/C snv 0.20 1
rs9894946
TP53
0.925 0.160 17 7667762 intron variant A/C;G snv 2
rs9892622 1.000 0.080 17 78350041 downstream gene variant G/A snv 0.50 1
rs988712
BDNF-AS
0.925 0.160 11 27541835 intron variant G/A;T snv 2
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 10
rs9825174
XXYLT1
0.925 0.120 3 195118855 intron variant C/A;G;T snv 2
rs9816226
DGKG
1.000 0.080 3 186116710 intron variant A/T snv 0.82 5
rs9794
PPARD
0.882 0.200 6 35428018 3 prime UTR variant G/A;C;T snv 4
rs979012 1.000 0.080 20 6642727 intergenic variant T/C snv 0.67 6
rs9719268
INSIG1
1.000 0.080 7 155306928 intron variant G/T snv 0.12 1
rs9606756
TCN2
0.790 0.160 22 30610873 missense variant A/G snv 0.12 0.14 7
rs9568867 1.000 0.080 13 53533217 intron variant G/A snv 0.13 2
rs9568856 1.000 0.080 13 53490846 intron variant G/A;C snv 1
rs955383
LMNA
1.000 0.080 1 156112239 intron variant G/A;C snv 1
rs9471077
KIF6 ; LOC105375047
1.000 0.080 6 39340966 intron variant A/G snv 0.51 1
rs9470387
CPNE5
1.000 0.080 6 36746081 intron variant C/A snv 0.27 1
rs9470386
CPNE5
0.925 0.160 6 36745943 intron variant G/A;C snv 2
rs9462535
KIF6
1.000 0.080 6 39348016 intron variant C/A;T snv 1
rs9450898
CNR1
0.925 0.160 6 88154344 intron variant C/T snv 0.21 3
rs9444584
CNR1
0.882 0.160 6 88152840 intron variant C/T snv 0.30 4
rs943003
ENPP1
0.882 0.120 6 131819872 non coding transcript exon variant C/T snv 0.64 3
rs942758928
MC4R
1.000 0.080 18 60371854 missense variant C/T snv 8.0E-06 1.4E-05 2
rs939583 1.000 0.080 2 622531 intergenic variant C/T snv 0.85 4