Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9261290
RNF39
0.807 0.280 6 30070870 3 prime UTR variant T/C;G snv 5.2E-02; 7.2E-06 10
rs185819
TNXB
0.851 0.200 6 32082290 missense variant T/A;C;G snv 8.2E-06; 0.58; 4.1E-06 8
rs2516448 0.827 0.120 6 31422633 intron variant T/C;G snv 7
rs2844511 0.807 0.200 6 31422007 intron variant A/G;T snv 7
rs527476195
PSORS1C1
0.925 0.120 6 31133165 intron variant G/A snv 6
rs12211410
TNXB
0.925 0.120 6 32081646 missense variant C/G;T snv 5.6E-05; 7.7E-02; 3.7E-05 5
rs1265115
CCHCR1
0.925 0.080 6 31149298 non coding transcript exon variant C/A;T snv 5
rs1894406
HLA-DOB
0.925 0.120 6 32819279 intron variant C/G;T snv 5
rs241440
TAP2
0.925 0.120 6 32829584 intron variant C/G;T snv 0.30 5
rs2534678
MICB ; MICB-DT
0.925 0.120 6 31496186 intron variant G/A;T snv 5
rs2621373 0.925 0.120 6 32797353 TF binding site variant T/A;C;G snv 5
rs2844529 0.925 0.120 6 31385816 upstream gene variant G/A;T snv 5
rs2844795
TRIM31 ; TRIM31-AS1
0.925 0.120 6 30106070 intron variant C/G;T snv 5
rs3130424 0.925 0.040 6 31250462 intergenic variant A/C;G;T snv 5
rs3130779 0.925 0.080 6 30904426 upstream gene variant A/C;G;T snv 5
rs3130981
CDSN ; PSORS1C1
0.925 0.080 6 31116036 missense variant T/C;G snv 0.76 5
rs3131009
PSORS1C1
0.925 0.080 6 31131055 intron variant G/A;C snv 5
rs429150
TNXB
1.000 6 32107786 intron variant T/C;G snv 5
rs528878831
PSORS1C1
0.925 0.080 6 31131055 intron variant G/A;C snv 5
rs540385376
PSORS1C1 ; CDSN
0.925 0.120 6 31117605 non coding transcript exon variant C/A snv 5
rs554543329 1.000 6 30971106 intergenic variant A/G snv 5
rs7382297
HLA-B
0.925 0.080 6 31279290 intron variant T/C;G snv 5
rs10947091
HCG20
1.000 6 30779439 intron variant C/G;T snv 4
rs111182473 1.000 6 31385912 upstream gene variant G/A;T snv 4
rs1128175
PSORS1C3
1.000 6 31182658 upstream gene variant A/G;T snv 4