Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9991328
FAM13A
4 88791970 intron variant C/T snv 0.53 5
rs9988
GGA3 ; NUP85
17 75234761 synonymous variant C/T snv 0.86 0.85 1
rs998749
MECOM
3 169255014 intron variant A/G snv 0.40 1
rs998732
TM6SF2
19 19267862 intron variant A/G snv 0.16 1
rs998584 6 43790159 downstream gene variant C/A snv 0.41 11
rs9976841
KCNJ6 ; DSCR4
21 38112229 intron variant G/A snv 0.45 1
rs9942009 3 89072771 intergenic variant C/T snv 0.41 1
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 10
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9932957 16 11539171 intergenic variant A/G;T snv 1
rs9932196
TMEM219
16 29971798 3 prime UTR variant G/T snv 0.42 1
rs9931989
ATP2A1
16 28894763 intron variant G/C snv 0.68 4
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 16
rs9923544
FTO
1.000 0.080 16 53768073 intron variant C/T snv 0.42 3
rs9907033
LOC101927389
17 55638089 intergenic variant T/C snv 0.38 1
rs9905388
TIMP2
17 78906167 intron variant T/C snv 0.42 1
rs9896963
ZZEF1
17 4063297 intron variant T/C;G snv 1
rs9893691
UBE2G1
17 4282329 intron variant C/T snv 0.57 1
rs9878908 3 12260963 upstream gene variant C/T snv 0.83 1
rs987763
LOC105377989
6 126960402 intron variant C/A;T snv 1
rs9872754
MRAS
3 138399143 intron variant C/T snv 0.12 1
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 10
rs9872031 3 12454962 regulatory region variant G/A snv 0.37 1
rs9860730
ADAMTS9-AS2
3 64715470 intron variant A/G snv 0.50 3
rs9844972 1.000 0.080 3 150379848 regulatory region variant G/A;C snv 4