Source: GWASDB ×
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 24
rs653178
ATXN2
0.672 0.600 12 111569952 intron variant C/T snv 0.67 17
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 14
rs2476601
AP4B1-AS1 ; PTPN22
0.498 0.800 1 113834946 missense variant A/G snv 0.93 0.93 13
rs11065987 0.807 0.280 12 111634620 intergenic variant A/G snv 0.29 12
rs17696736
NAA25
0.827 0.240 12 112049014 intron variant A/G snv 0.30 11
rs2516049
HLA-DRB1
0.742 0.400 6 32602623 intergenic variant T/C snv 0.27 9
rs477515
HLA-DRB1
0.790 0.400 6 32601914 intergenic variant G/A snv 0.27 7
rs3087243
CTLA4
0.623 0.720 2 203874196 downstream gene variant G/A snv 0.37 6
rs6679677
PHTF1
0.653 0.320 1 113761186 upstream gene variant C/A snv 6.7E-02 6
rs925489
PTCSC2
0.882 0.080 9 97784318 intron variant C/T snv 0.71 5
rs3129720 0.851 0.280 6 32695854 intergenic variant T/C snv 0.76 4
rs10774625
ATXN2
0.763 0.320 12 111472415 intron variant A/G snv 0.66 4
rs11066188
HECTD4
0.851 0.320 12 112172910 intron variant G/A;C snv 0.30; 4.1E-06 4
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 4
rs11066320
PTPN11
0.925 0.120 12 112468611 intron variant A/G snv 0.70 4
rs34536443
TYK2
0.667 0.400 19 10352442 missense variant G/C snv 2.7E-02 2.8E-02 4
rs4409785 0.752 0.240 11 95578258 intron variant T/C snv 0.13 3
rs6906021
HLA-DQB1-AS1
0.827 0.320 6 32658534 upstream gene variant T/C snv 0.47 3
rs10759944
PTCSC2
0.925 0.080 9 97794690 intron variant A/G snv 0.72 3
rs1443438
PTCSC2
0.827 0.080 9 97787746 intron variant T/A;C snv 3
rs7850258
PTCSC2
0.827 0.200 9 97786731 intron variant A/G snv 0.72 3
rs6910071
TSBP1 ; TSBP1-AS1
0.790 0.320 6 32315077 intron variant A/G snv 0.14 3
rs10984103 0.925 0.080 9 97876993 TF binding site variant A/C snv 0.68 2
rs12191243 1.000 0.040 6 135125688 intergenic variant C/G snv 0.20 2