Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1980493
BTNL2 ; TSBP1-AS1
0.776 0.400 6 32395438 intron variant T/C snv 0.13 6
rs3763313
BTNL2
0.807 0.320 6 32408694 upstream gene variant A/C snv 0.21 5
rs3806156
BTNL2 ; TSBP1-AS1
0.827 0.280 6 32405921 intron variant G/A;T snv 5
rs3817963
TSBP1-AS1 ; BTNL2
0.776 0.360 6 32400310 intron variant T/C snv 0.25 5
rs2076530
TSBP1-AS1 ; BTNL2
0.724 0.640 6 32396039 missense variant T/C snv 0.42 0.40 5
rs10947261
BTNL2 ; TSBP1-AS1
0.882 0.240 6 32405455 splice region variant G/T snv 0.11 4
rs9268480
BTNL2 ; TSBP1-AS1
0.882 0.200 6 32396067 synonymous variant C/T snv 0.26 0.24 3
rs2076533
BTNL2 ; TSBP1-AS1
0.882 0.200 6 32395750 intron variant C/T snv 0.40 3
rs3763309
TSBP1-AS1 ; BTNL2
0.882 0.160 6 32408196 upstream gene variant C/A;T snv 3
rs3763307
TSBP1-AS1 ; BTNL2
0.882 0.200 6 32406845 non coding transcript exon variant A/T snv 0.24 3
rs3793126
TSBP1-AS1 ; BTNL2
0.882 0.240 6 32403842 intron variant A/G snv 0.24 3
rs3763316
BTNL2
0.925 0.160 6 32408969 upstream gene variant C/T snv 0.24 2
rs9268491
BTNL2 ; TSBP1-AS1
0.925 0.160 6 32406354 non coding transcript exon variant C/G;T snv 2
rs2076524
BTNL2 ; TSBP1-AS1
0.925 0.160 6 32402907 intron variant A/G snv 0.26 0.24 2
rs28362683
BTNL2 ; TSBP1-AS1
1.000 0.040 6 32405186 synonymous variant G/A snv 0.12 0.10 2
rs2294881
BTNL2 ; TSBP1-AS1
1.000 0.040 6 32399827 intron variant T/C snv 0.19 2
rs3817973
HCG23 ; BTNL2 ; TSBP1-AS1
0.925 0.200 6 32393334 intron variant C/T snv 0.39 2
rs2076525
TSBP1-AS1 ; BTNL2
0.925 0.160 6 32402839 intron variant T/C snv 0.24 2
rs2076529
TSBP1-AS1 ; BTNL2
1.000 0.120 6 32396178 synonymous variant T/C snv 0.41 0.39 2
rs2076522
TSBP1-AS1 ; BTNL2
0.925 0.160 6 32403402 intron variant G/C;T snv 2
rs3117116
TSBP1-AS1 ; BTNL2
1.000 0.040 6 32399240 intron variant G/A snv 0.87 2
rs2294882
TSBP1-AS1 ; BTNL2
6 32399738 intron variant T/C snv 0.19 2
rs10947262
TSBP1-AS1 ; BTNL2
0.925 0.040 6 32405535 non coding transcript exon variant C/T snv 0.12 2
rs9268503
BTNL2
1.000 0.040 6 32409284 upstream gene variant C/T snv 0.55 1
rs9268502
BTNL2
1.000 0.040 6 32409155 upstream gene variant C/T snv 0.55 1