Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7642134 3 86867732 intergenic variant A/G snv 0.55 1
rs7665931 4 103739525 intergenic variant C/T snv 9.7E-02 1
rs7821178 0.925 0.080 8 77181601 intergenic variant C/A;G;T snv 1
rs8014131 14 85497512 intron variant C/A snv 0.41 1
rs900145 11 13272358 upstream gene variant C/T snv 0.62 1
rs9555810 13 111529090 intergenic variant C/G;T snv 1
rs9635759 17 51536424 regulatory region variant G/A snv 0.25 1
rs320320
AKT3
1 243671884 intron variant A/G snv 0.30 1
rs6575793
BEGAIN
14 100565880 intron variant T/C snv 0.55 1
rs2479724
BYSL
6 41923244 intron variant T/C snv 0.62 1
rs17268785
CCDC85A
2 56364948 intron variant A/G snv 0.20 1
rs1361108
CENPW
6 126446454 intron variant C/T snv 0.44 1
rs10423674
CRTC1
19 18707093 intron variant C/A;T snv 1
rs17669535
DLGAP2 ; LOC286083
8 1295964 intron variant C/G snv 7.4E-02 1
rs3914188
EEF1AKMT4-ECE2 ; ECE2
3 184292260 3 prime UTR variant G/C snv 0.73 0.73 1
rs2687729
EEFSEC
3 128176383 intron variant A/G snv 0.30 1
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 11
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 10
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 4
rs10899489
GAB2
11 78384327 non coding transcript exon variant C/A;T snv 1
rs4693089
HELQ
4 83452469 intron variant A/G snv 0.60 1
rs2277339
HSD17B6 ; PRIM1
12 56752285 missense variant T/G snv 0.12 0.14 1
rs757647
KDM3B
5 138371626 intron variant G/A;C snv 1
rs7617480
KLHDC8B
3 49173299 intron variant A/C snv 0.76 1
rs314277
LIN28B
0.925 0.080 6 104959787 intron variant A/C;G;T snv 3