Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs629301
CELSR2
0.851 0.120 1 109275684 3 prime UTR variant G/T snv 0.74 19
rs61824877
LINC00862
1 200273504 intron variant G/A snv 0.11 3
rs9943291
HMGCS2
1 119749667 intron variant T/G snv 8.2E-02 3
rs477992
PHGDH
1 119714953 intron variant A/G snv 0.69 2
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 1
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 1
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
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 18
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 17
rs222826 0.851 0.120 2 146120964 regulatory region variant T/C snv 0.94 16
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 16
rs6759518
SLC30A3
0.851 0.120 2 27263727 intron variant G/C snv 5.5E-02 16
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 9
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 8
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 7
rs2232326
SPC25 ; G6PC2
2 168907981 missense variant T/C snv 5.1E-03 3.3E-03 3
rs12053049
SPC25
2 168910638 intron variant T/C snv 5.2E-02 2
rs12712928 2 44964941 intron variant G/C snv 0.18 2
rs1349497
RAPGEF4-AS1
2 172727935 intron variant G/A;C snv 2
rs7632505
SEMA5B
0.827 0.120 3 123019460 intron variant A/G snv 0.34 16
rs11924032
SLC2A2
3 171017310 intron variant G/A snv 0.29 3
rs11705729
IGF2BP2
1.000 0.080 3 185789511 intron variant A/T snv 0.45 2
rs13114738
SLC39A8
0.851 0.120 4 102363708 intron variant C/A;T snv 16
rs1869717
MAML3
0.851 0.120 4 139829967 intron variant G/C snv 0.14 16