Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs548291389 16 67970889 upstream gene variant T/G snv 2.2E-04 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs4939883
LOC105372112
1.000 0.040 18 49640844 TF binding site variant T/C;G snv 3
rs4407894 8 20076385 upstream gene variant T/C;G snv 2
rs13379043
MIDEAS
14 73783423 intron variant T/C;G snv 1
rs2293889
TRPS1
8 115586972 intron variant T/C;G snv 2.0E-04; 0.65 1
rs7013777 1.000 0.040 8 20020845 intergenic variant T/C;G snv 1
rs79407615 8 19992588 intergenic variant T/C;G snv 1
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 35
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 26
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 22
rs174547
FADS2 ; FADS1
0.742 0.240 11 61803311 intron variant T/C snv 0.28 20
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 17
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs6533530 0.851 0.120 4 110810780 intergenic variant T/C snv 0.47 16
rs11727676
HHIP
0.776 0.080 4 144737912 synonymous variant T/C snv 6.6E-02 6.4E-02 14
rs102275
TMEM258
0.827 0.320 11 61790331 non coding transcript exon variant T/C snv 0.47 10
rs1421085
FTO
0.752 0.280 16 53767042 intron variant T/C snv 0.31 10
rs17451107 3 157079820 upstream gene variant T/C snv 0.38 7
rs174550
FADS1 ; FADS2
0.925 0.160 11 61804006 5 prime UTR variant T/C snv 0.28 7
rs7607980
COBLL1
1.000 0.080 2 164694691 missense variant T/C snv 0.11 0.13 7
rs10408163
ZC3H4
19 47093845 non coding transcript exon variant T/C snv 0.52 6
rs174529
MYRF ; TMEM258
11 61776489 intron variant T/C snv 0.34 6
rs174551
FADS1 ; FADS2
11 61806212 5 prime UTR variant T/C snv 0.28 6
rs2043085
ALDH1A2
0.827 0.080 15 58388755 intron variant T/C snv 0.54 6