Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10173355
UGT1A9 ; UGT1A7 ; UGT1A10 ; UGT1A8
1.000 2 233688675 intron variant A/G;T snv 1
rs1042126
CDSN ; PSORS1C1
1.000 6 31116511 synonymous variant T/C snv 0.57 0.58 4
rs1042134
CDSN ; PSORS1C1
1.000 6 31115887 3 prime UTR variant G/A snv 0.58 4
rs1042147
CDSN ; PSORS1C1
1.000 6 31115379 3 prime UTR variant A/G snv 0.58 4
rs10456057
HLA-B ; USP8P1
1.000 6 31277757 non coding transcript exon variant A/C;G;T snv 0.13 4
rs10484554
LOC112267902 ; HLA-B
0.807 0.200 6 31306778 intron variant C/T snv 0.12 8
rs10501678
GRM5
1.000 11 88708934 intron variant C/T snv 3.1E-02 4
rs1051794
MICA
0.925 0.120 6 31411332 missense variant G/A snv 0.34 0.35 4
rs1058026
HLA-B
0.925 0.120 6 31353908 3 prime UTR variant A/C snv 0.21 5
rs1062470
PSORS1C1 ; CDSN
0.925 0.040 6 31116658 synonymous variant G/A snv 0.37 0.41 4
rs10947091
HCG20
1.000 6 30779439 intron variant C/G;T snv 4
rs10947095
HCG20
1.000 6 30789798 intron variant C/T snv 0.35 4
rs10947207 1.000 6 31393708 downstream gene variant T/C snv 0.31 5
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
rs11753208 1.000 6 31037655 downstream gene variant C/T snv 9.7E-02 4
rs11758688
HCG20
1.000 6 30790571 intron variant C/T snv 0.35 4
rs12122100
LOC728989 ; NBPF13P
1.000 1 147037378 intron variant T/C snv 0.76 4
rs12153855
TNXB
0.776 0.320 6 32107027 intron variant T/C snv 0.11 10
rs12185555 1.000 2 226694601 regulatory region variant A/G snv 0.25 4
rs12190030
HCG21 ; SFTA2 ; MUCL3
1.000 6 30953587 3 prime UTR variant C/T snv 0.21 4
rs12191877
HLA-B
0.851 0.120 6 31285148 intron variant C/T snv 0.12 5
rs12198173
TNXB
0.827 0.240 6 32059031 intron variant G/A snv 0.10 9
rs12207756
PSORS1C1 ; CDSN
1.000 6 31118905 intron variant C/T snv 0.14 4
rs12211410
TNXB
0.925 0.120 6 32081646 missense variant C/G;T snv 5.6E-05; 7.7E-02; 3.7E-05 5