Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs999947969
CD36
0.827 0.080 7 80671145 synonymous variant C/T snv 7
rs9989419 0.882 0.120 16 56951227 regulatory region variant A/G snv 0.55 11
rs9982601 0.851 0.080 21 34226827 intron variant C/T snv 0.15 4
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 98
rs9891572 1.000 0.040 17 2525214 intergenic variant C/T snv 0.17 3
rs9860747 0.925 0.080 3 186869628 regulatory region variant T/C snv 0.70 2
rs9818870
MRAS
0.807 0.200 3 138403280 3 prime UTR variant C/A;T snv 9
rs9815354
ULK4
0.925 0.160 3 41871159 intron variant G/A;T snv 4
rs9797861
SLC44A2
0.790 0.200 19 10632450 intron variant C/A;G;T snv 9
rs974819 0.807 0.080 11 103789839 intron variant T/A;C snv 6
rs972655070
TSTD1 ; USF1
0.882 0.040 1 161040282 missense variant G/A snv 4.0E-06 1.4E-05 3
rs965384857
LPL
0.827 0.160 8 19954234 missense variant G/A snv 4.0E-06 5
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs958546
LRRC63
0.882 0.040 13 46259582 intron variant G/C snv 0.29 3
rs9534275
BRCA2
0.851 0.080 13 32366208 intron variant C/A snv 0.52 7
rs9508025
FLT1
0.925 0.040 13 28409926 intron variant C/G;T snv 2
rs9468076
ZNF204P
1.000 0.040 6 27371111 upstream gene variant C/T snv 0.16 1
rs9465871
CDKAL1
0.882 0.120 6 20717024 intron variant T/C snv 0.30 4
rs9461366 1.000 0.040 6 27342754 intergenic variant G/A snv 0.31 1
rs9461362 1.000 0.040 6 27336148 intergenic variant C/T snv 0.13 1
rs9461249
BTN2A2
1.000 0.040 6 26383158 5 prime UTR variant T/C snv 0.23 1
rs944797
CDKN2B-AS1
0.882 0.120 9 22115287 intron variant T/C;G snv 0.49 5
rs9395208
PLA2G7
1.000 0.040 6 46735582 5 prime UTR variant G/C snv 0.20 1
rs939348
THRA
0.851 0.240 17 40075600 intron variant T/C;G snv 5
rs9389154
SGK1
0.882 0.120 6 134293623 intron variant G/A snv 0.11 4