Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 35
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 21
rs7412
APOE
0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 20
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 18
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
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 18
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 17
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 16
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 16
rs3764261 0.732 0.280 16 56959412 upstream gene variant C/A snv 0.31 13
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
rs738409
PNPLA3
0.557 0.720 22 43928847 missense variant C/G snv 0.28 0.22 11
rs651821
APOA5
0.851 0.360 11 116791863 5 prime UTR variant C/T snv 0.88 0.89 10
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 10
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs7138803 0.827 0.240 12 49853685 intergenic variant G/A;T snv 9
rs8050136
FTO
0.716 0.560 16 53782363 intron variant C/A snv 0.40 9