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
rs1047891
CPS1
0.827 0.200 2 210675783 missense variant C/A snv 0.30 0.33 25
rs79105258
CUX2
12 111280427 intron variant C/A;T snv 23
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 18
rs780093
GCKR
0.763 0.240 2 27519736 intron variant T/C snv 0.68 16
rs6058093
PIGU
0.776 0.080 20 34625392 intron variant A/C snv 0.55 12
rs715
CPS1
1.000 0.040 2 210678331 3 prime UTR variant T/C snv 0.28 10
rs10857147 1.000 0.040 4 80259918 intergenic variant A/T snv 0.25 9
rs62435145 1.000 0.040 7 1246931 regulatory region variant G/T snv 0.51 8
rs963837
LOC101928338 ; LINC02859
0.925 0.120 11 30727543 intergenic variant T/C snv 0.35 8
rs9895661
BCAS3
0.882 0.200 17 61379228 non coding transcript exon variant C/T snv 0.69 7
rs77924615
PDILT
1.000 0.080 16 20381010 intron variant G/A snv 0.16 7
rs1533988 7 1253374 intergenic variant A/T snv 0.59 6
rs17216707 20 54115823 intergenic variant T/C snv 0.17 6
rs3925584
LOC101928338
1.000 0.080 11 30738788 intergenic variant T/C snv 0.35 6
rs17050272
LOC105373585
0.882 0.120 2 120548864 upstream gene variant G/A snv 0.33 6
rs9472135
LOC107986598
0.925 0.120 6 43842065 intron variant T/A;C;G snv 6
rs13146355
SHROOM3
1.000 0.040 4 76490987 intron variant G/A snv 0.33 6
rs6127099 20 54114863 intergenic variant A/T snv 0.28 5
rs7422339
CPS1
1.000 0.080 2 210675783 missense variant C/A snv 5
rs3741414
INHBC
0.925 0.120 12 57450266 3 prime UTR variant C/T snv 0.19 5
rs186459505
SFMBT1
0.925 0.120 3 52907083 missense variant G/A;T snv 1.1E-04; 4.0E-06 5
rs149454410
SLC2A9
0.925 0.120 4 9942000 missense variant C/G;T snv 4.0E-05; 3.2E-04 5
rs8068318
TBX2
17 61406405 non coding transcript exon variant C/T snv 0.56 5
rs12917707
UMOD
0.827 0.200 16 20356368 upstream gene variant G/T snv 0.14 5