Source: GWASDB ×
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 8
rs211718
SLC44A5
1 75640990 downstream gene variant T/C snv 0.75 3
rs2794520 0.807 0.240 1 159709026 upstream gene variant C/A;T snv 3
rs10799701 1 21494497 intergenic variant A/G snv 0.47 2
rs12753193 1 65703996 non coding transcript exon variant G/A snv 0.58 2
rs477992
PHGDH
1 119714953 intron variant A/G snv 0.69 2
rs9332998
CYP4A11
1 46938514 intron variant T/C snv 0.16 2
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 25
rs780094
GCKR
0.658 0.400 2 27518370 intron variant T/C snv 0.67 24
rs673548
APOB
0.925 0.120 2 21014672 intron variant G/A;T snv 10
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 7
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 6
rs887829
UGT1A8 ; UGT1A5 ; UGT1A6 ; UGT1A7 ; UGT1A4 ; UGT1A3 ; UGT1A10 ; UGT1A1 ; UGT1A9
0.763 0.280 2 233759924 intron variant C/T snv 0.36 6
rs13391552
ALMS1
2 73591809 intron variant G/A;C snv 2
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 2
rs2216405 2 210752170 intergenic variant A/G snv 0.15 2
rs478442 0.851 0.120 2 21176344 intergenic variant G/C;T snv 2
rs11705729
IGF2BP2
1.000 0.080 3 185789511 intron variant A/T snv 0.45 1
rs4481233
SLC2A9
0.925 0.120 4 9954455 intron variant C/T snv 0.16 5
rs4253252
KLKB1
4 186236304 intron variant T/G snv 0.56 3
rs8396
ETFDH ; PPID
4 158709665 3 prime UTR variant T/C snv 0.29 3
rs2087160
ENPEP
4 110413574 intron variant G/T snv 0.68 2
rs7703051 0.851 0.120 5 75329662 intron variant C/A snv 0.38 3
rs272889
SLC22A4 ; MIR3936HG
5 132329685 intron variant A/G snv 0.64 2
rs7760535
REV3L ; MFSD4B
6 111425880 intron variant G/C snv 0.46 3