Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs998584 6 43790159 downstream gene variant C/A snv 0.41 4
rs9940128
FTO
0.851 0.120 16 53766842 intron variant G/A snv 0.42 6
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs9931989
ATP2A1
16 28894763 intron variant G/C snv 0.68 3
rs9930506
FTO
0.776 0.360 16 53796553 intron variant A/G snv 0.36 5
rs9923544
FTO
1.000 0.080 16 53768073 intron variant C/T snv 0.42 2
rs987763
LOC105377989
6 126960402 intron variant C/A;T snv 1
rs987237
TFAP2B
0.925 0.120 6 50835337 intron variant A/G snv 0.17 3
rs984222
TBX15
1 118961220 intron variant C/A;G snv 1
rs9750952 1.000 0.080 2 238827723 intergenic variant C/T snv 0.19 1
rs9647379
FNDC3B
3 172067378 intron variant G/C snv 0.32 1
rs9515201
COL4A2
0.925 0.080 13 110388451 intron variant A/C snv 0.63 1
rs9491696
RSPO3
6 127131494 intron variant C/G snv 0.45 1
rs9369425
LOC107986598
0.882 0.160 6 43843237 downstream gene variant G/A snv 0.66 3
rs9302652
FTO
1.000 0.080 16 53832063 intron variant C/T snv 0.74 1
rs900400
LINC02029
0.925 0.080 3 157080986 upstream gene variant T/C snv 0.36 1
rs887912 1.000 0.080 2 59075742 intron variant T/C;G snv 3
rs8070723
MAPT
0.851 0.240 17 46003698 intron variant A/G snv 0.18 5
rs7797307 7 69221140 intron variant G/C snv 7.6E-02 1
rs7776725
FAM3C
1.000 0.080 7 121393067 intron variant T/C snv 0.28 2
rs7745274
RSPO3 ; LOC112267972
6 127188012 intron variant G/A snv 0.56 1
rs7647305
DGKG
1.000 0.080 3 186116501 intron variant T/C snv 0.74 3
rs7637773
IGF2BP2
1.000 0.080 3 185797847 intron variant G/A snv 0.38 1
rs757608 17 61419916 regulatory region variant A/G;T snv 1
rs7498665
SH2B1
0.925 0.120 16 28871920 missense variant A/G;T snv 0.35 5