Source: GWASDB ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13394720 1.000 2 233593475 intergenic variant T/C snv 7.0E-02 6
rs13437082 1.000 6 31386783 upstream gene variant C/T snv 0.32 6
rs10947207 1.000 6 31393708 downstream gene variant T/C snv 0.31 5
rs2256175
MICA
1.000 6 31412672 intron variant C/T snv 0.55 5
rs2844615
HLA-B
1.000 6 31275182 intron variant C/T snv 0.11 5
rs3819299
HLA-B
1.000 6 31354590 non coding transcript exon variant T/G snv 7.7E-02 2.3E-02 5
rs429150
TNXB
1.000 6 32107786 intron variant T/C;G snv 5
rs4711268 1.000 6 31386727 upstream gene variant C/T snv 0.31 5
rs4711269 1.000 6 31387042 upstream gene variant C/T snv 0.32 5
rs554543329 1.000 6 30971106 intergenic variant A/G snv 5
rs6932730 0.925 6 31386405 upstream gene variant T/C snv 0.26 5
rs7751505 1.000 6 31392478 downstream gene variant A/C snv 0.31 5
rs7751725 1.000 6 31392656 downstream gene variant A/G snv 0.31 5
rs7756521
DDR1
1.000 6 30880476 intron variant T/C snv 0.25 5
rs9380238
LOC112267902 ; HLA-B ; LINC02571
1.000 6 31299841 intron variant A/G snv 0.15 5
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
rs10501678
GRM5
1.000 11 88708934 intron variant C/T snv 3.1E-02 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
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