Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs560887
SPC25 ; G6PC2
0.827 0.120 2 168906638 intron variant T/C snv 0.79 0.80 9
rs2442719
HLA-B
0.882 0.120 6 31352761 intron variant C/T snv 0.53 5
rs1265564
CUX2
1.000 0.120 12 111270654 non coding transcript exon variant A/C snv 0.30 4
rs3842727
TH
1.000 0.120 11 2163618 upstream gene variant G/T snv 0.58 3
rs428595
LOC107985532
1.000 0.120 22 21662102 non coding transcript exon variant A/G snv 0.98 3
rs9273368
HLA-DQB1-AS1
0.882 0.120 6 32658698 upstream gene variant G/A snv 0.23 3
rs1015166
TAP2
0.925 0.120 6 32830954 intron variant C/G;T snv 0.28 2
rs1264622
HLA-L ; HCG18 ; HCG17
1.000 0.120 6 30289159 non coding transcript exon variant C/T snv 0.13 2
rs151234
CLN3 ; APOBR
1.000 0.120 16 28494339 5 prime UTR variant G/A;C snv 2
rs2249742
HLA-B ; HLA-C
0.925 0.120 6 31272944 intron variant C/T snv 0.50 2
rs2358994
BCL2L15 ; AP4B1-AS1
0.925 0.120 1 113886839 intron variant G/A snv 0.16 2
rs3135002 1.000 0.120 6 32700662 TF binding site variant A/C snv 0.80 2
rs34593439
CTSH
1.000 0.120 15 78942615 intron variant G/A;C snv 0.10 2
rs559047 1.000 0.120 1 238590616 intergenic variant T/A;C snv 2
rs6043409
SIRPG ; SIRPG-AS1
1.000 0.120 20 1635560 missense variant A/G snv 0.73 0.72 2
rs61211515 1.000 0.120 6 30133199 upstream gene variant TT/-;T;TTT;TTTT delins 0.14 2
rs7111341 0.925 0.120 11 2191936 regulatory region variant C/T snv 0.29 2
rs7679475
LOC107986309
0.925 0.120 4 121392885 intergenic variant A/C;G snv 2
rs9260151
HLA-A
1.000 0.120 6 29943253 non coding transcript exon variant C/T snv 0.16 0.14 2
rs927292
ZFP36L1
1.000 0.120 14 68792124 intron variant C/G snv 0.68 2
rs10277986 1.000 0.120 7 50961290 intron variant T/A;C snv 1
rs10786436
HPSE2
1.000 0.120 10 98540425 intron variant C/T snv 0.40 1
rs11052552
LINC02390
1.000 0.120 12 9703362 upstream gene variant T/G snv 0.42 1
rs11170445 1.000 0.120 12 53151908 upstream gene variant C/T snv 0.33 1
rs11203202
UBASH3A
1.000 0.120 21 42405248 intron variant C/G;T snv 1