Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs1333049
CDKN2B-AS1
0.614 0.520 9 22125504 intron variant G/C snv 0.41 18
rs1535
FADS2
0.752 0.240 11 61830500 intron variant A/G snv 0.31 18
rs9939609
FTO
0.559 0.720 16 53786615 intron variant T/A snv 0.41 18
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs11066280
HECTD4
0.742 0.280 12 112379979 intron variant T/A snv 7.0E-03 13
rs1558902
FTO
0.827 0.120 16 53769662 intron variant T/A snv 0.31 12
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 10
rs2074356
HECTD4
0.763 0.280 12 112207597 intron variant G/A snv 3.8E-03 9
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 9
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9
rs4148325
UGT1A8 ; UGT1A5 ; UGT1A10 ; UGT1A7 ; UGT1A1 ; UGT1A9 ; UGT1A3 ; UGT1A4 ; UGT1A6
0.851 0.080 2 233764663 intron variant C/T snv 0.36 8
rs1333048
CDKN2B-AS1
0.683 0.320 9 22125348 intron variant A/C snv 0.44 7
rs1532085
ALDH1A2
0.882 0.080 15 58391167 intron variant A/G;T snv 7
rs17863787
UGT1A9 ; UGT1A8 ; UGT1A6 ; UGT1A7 ; UGT1A10
0.925 0.040 2 233702448 intron variant T/G snv 0.30 7
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 7
rs6993770
ZFPM2 ; ZFPM2-AS1
0.925 0.080 8 105569300 intron variant A/T snv 0.31 7
rs929596
UGT1A5 ; UGT1A4 ; UGT1A9 ; UGT1A10 ; UGT1A8 ; UGT1A7 ; UGT1A6 ; UGT1A3 ; UGT1A1
0.925 0.040 2 233765830 intron variant A/G snv 0.32 7
rs10468017
ALDH1A2
0.851 0.120 15 58386313 intron variant C/T snv 0.24 6
rs1883025
ABCA1
0.807 0.120 9 104902020 intron variant C/T snv 0.28 6
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54 6
rs11708067
ADCY5
0.882 0.080 3 123346931 intron variant A/G snv 0.19 5
rs12686004
ABCA1
1.000 0.040 9 104891145 intron variant G/A snv 9.1E-02 5