Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2071538
TAP1 ; PSMB9
0.925 0.160 6 32850901 intron variant G/A snv 0.18 0.17 2
rs2071540
TAP1 ; PSMB9 ; PSMB8-AS1 ; PSMB8
0.925 0.200 6 32845139 non coding transcript exon variant T/C snv 0.61 2
rs991760
TAP1 ; PSMB9
1.000 0.120 6 32855790 intron variant G/A snv 8.2E-02 1
rs2071481
TAP1 ; PSMB9
1.000 0.120 6 32852088 intron variant T/C snv 0.14 0.11 1
rs4148882
TAP1 ; PSMB9
1.000 0.080 6 32849181 non coding transcript exon variant G/A snv 0.71 1