Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 61
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 55
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 34
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 23
rs635634 0.882 0.160 9 133279427 upstream gene variant T/A;C snv 17
rs1800961
HNF4A
0.851 0.160 20 44413724 missense variant C/T snv 3.1E-02 2.5E-02 17
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15
rs35188965
SLC12A7
5 1104823 intron variant C/G;T snv 12
rs2814778
CADM3-AS1 ; ACKR1
0.763 0.360 1 159204893 5 prime UTR variant T/C snv 0.25 11
rs9977672 0.827 0.120 21 39091357 intergenic variant G/A snv 0.22 10
rs218265 4 54542832 intergenic variant T/C snv 0.21 9
rs445
CDK6
7 92779056 intron variant C/T snv 0.14 9
rs150813342
GFI1B
9 132989126 synonymous variant C/T snv 4.1E-03 4.1E-03 9
rs2954031 8 125479491 intron variant G/T snv 0.42 8
rs6740847 0.925 0.040 2 181443625 intergenic variant A/G snv 0.57 8
rs6782228 3 128604581 intergenic variant G/C snv 0.28 7
rs34599082
ACKR1 ; CADM3-AS1
1 159205704 missense variant C/T snv 1.1E-02 9.9E-03 7
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24 7
rs143034248
JAML
11 118210555 missense variant C/T snv 4.0E-03 3.5E-03 7
rs12239046
NLRP3
1 247438293 intron variant T/C snv 0.58 7
rs4760
PLAUR
1.000 0.080 19 43648948 missense variant A/G snv 0.12 0.11 7
rs12266014
PRTFDC1
10 24922362 intron variant C/T snv 0.26 7
rs2038700
STXBP6
14 24992783 intron variant T/C snv 0.53 7
rs385893 0.925 0.080 9 4763176 downstream gene variant T/C snv 0.44 6
rs9271588 0.925 0.200 6 32623176 TF binding site variant T/C snv 0.43 6