Gene: TAP2 ×
Source: GWASDB ×
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1015166
rs1015166
TAP2
1 0.925 0.120 6 32830954 intron variant C/G;T snv 0.28 0.800 1.000 1 2007 2015
dbSNP: rs2228397
rs2228397
TAP2
1 1.000 0.120 6 32832447 synonymous variant C/A snv 0.26 0.24 0.700 1.000 1 2007 2007
dbSNP: rs241424
rs241424
TAP2
2 0.925 0.200 6 32837157 intron variant G/A snv 0.50 0.700 1.000 1 2007 2007
dbSNP: rs241425
rs241425
TAP2
2 0.925 0.160 6 32837132 intron variant A/C;G snv 0.700 1.000 1 2007 2007
dbSNP: rs241427
rs241427
TAP2
2 0.925 0.160 6 32836637 intron variant A/G;T snv 0.700 1.000 1 2007 2007
dbSNP: rs241440
rs241440
TAP2
5 0.925 0.120 6 32829584 intron variant C/G;T snv 0.30 0.700 1.000 1 2007 2007
dbSNP: rs241447
rs241447
TAP2
5 0.827 0.280 6 32828974 missense variant T/C snv 0.31 0.26 0.700 1.000 1 2007 2007
dbSNP: rs241448
rs241448
TAP2
5 0.882 0.200 6 32828908 stop lost A/G snv 0.32 0.27 0.700 1.000 1 2007 2007
dbSNP: rs241452
rs241452
TAP2
5 0.925 0.120 6 32828569 3 prime UTR variant T/C snv 0.26 0.700 1.000 1 2007 2007
dbSNP: rs241453
rs241453
TAP2
5 0.882 0.160 6 32828449 3 prime UTR variant G/A snv 0.25 0.700 1.000 1 2007 2007
dbSNP: rs3763349
rs3763349
PSMB8 ; TAP2
1 1.000 0.120 6 32840455 upstream gene variant A/G snv 0.53 0.700 1.000 1 2007 2007
dbSNP: rs3819715
rs3819715
TAP2
1 1.000 0.120 6 32836442 intron variant G/A;T snv 0.700 1.000 1 2007 2007