Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1275561861
HLA-A
0.672 0.360 6 29944350 missense variant G/A snv 23
rs9260620
HLA-A
6 29955314 upstream gene variant T/G snv 0.24 7
rs199474387
HLA-A
0.807 0.240 6 29942870 missense variant G/C;T snv 6
rs3132685
HLA-A ; HCG9
0.807 0.320 6 29978172 intron variant G/A;T snv 6
rs2524005
HLA-A
0.882 0.160 6 29931900 upstream gene variant G/A snv 0.18 5
rs401618
HLA-A
0.827 0.120 6 29982433 downstream gene variant A/G;T snv 5
rs6904029
HLA-A ; HCG9
0.851 0.200 6 29975290 non coding transcript exon variant G/A snv 0.29 0.26 4
rs7758512
HLA-A ; ZNRD1ASP
1.000 6 30002812 intron variant T/G snv 0.17 4
rs1059536
HLA-A
1.000 0.080 6 29943448 missense variant A/C;G;T snv 4.1E-06; 0.17 3
rs3893464
HLA-A
1.000 0.120 6 29967473 downstream gene variant G/A snv 0.46 3
rs6457110
HLA-A
0.882 0.280 6 29966104 downstream gene variant T/A snv 0.40 3
rs768170742
HLA-A
1.000 0.080 6 29943448 frameshift variant ATGA/- del 1.9E-05 3
rs4313034
HLA-J ; ZNRD1ASP ; HLA-A
0.925 0.160 6 30006148 non coding transcript exon variant C/T snv 0.78 3
rs115625073
HCG4B ; HLA-A
1.000 0.040 6 29924456 upstream gene variant T/C snv 2
rs1128306
HCG9 ; HLA-A
0.925 0.120 6 29975492 non coding transcript exon variant G/A snv 0.22 2
rs2523946
HCG9 ; HLA-A
0.925 0.200 6 29974166 upstream gene variant C/A;G;T snv 2
rs2735076
HCG9 ; HLA-A
1.000 0.040 6 29975713 intron variant A/G snv 0.71 2
rs1061539
HLA-A
1.000 0.040 6 29969778 downstream gene variant T/A;C snv 2
rs111312615
HLA-A
1.000 0.040 6 29955302 upstream gene variant T/G snv 2
rs113205291
HLA-A
1.000 0.040 6 29894844 upstream gene variant A/G;T snv 2
rs114204022
HLA-A
1.000 0.040 6 29972902 upstream gene variant G/A snv 2
rs114577328
HLA-A
1.000 0.080 6 29959505 downstream gene variant G/C snv 1.3E-02 2
rs114950038
HLA-A
1.000 0.040 6 29983056 downstream gene variant G/A;C snv 2
rs115960997
HLA-A
1.000 0.040 6 29934332 downstream gene variant G/A;T snv 2
rs144304366
HLA-A
1.000 0.040 6 29936216 downstream gene variant T/C snv 2