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HLA » Haplotype Frequency Search
| Displaying all results from your selection. |  |
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| Line | Haplotype | Population | Frequency (%) | Sample Size | Location |
|---|---|---|---|---|---|
| 1 | A*26:01-B*35:01-C*03:03-DRB1*04:10-DQA1*03:03-DQB1*04:02-DPA1*02:02-DPB1*03:01 | Japan pop 17 | 0.33 | 3,078 | 37_36_N_138_2_E |
| 2 | A*26:01-B*35:01-C*03:03-DRB1*04:10 | Japan pop 16 | 0.30 | 18,604 | 35_41_N_139_46_E |
| 3 | A*02:01-B*35:01-C*03:03-DRB1*04:10 | Japan pop 16 | 0.18 | 18,604 | 35_41_N_139_46_E |
| 4 | A*02:01-B*35:01-C*03:03-DRB1*04:10-DQA1*03:03-DQB1*04:02-DPA1*01:03-DPB1*03:01 | Japan pop 17 | 0.07 | 3,078 | 37_36_N_138_2_E |
| 5 | A*11:01-B*35:01-C*03:03-DRB1*04:10-DQA1*03:03-DQB1*04:02-DPA1*02:02-DPB1*03:01 | Japan pop 17 | 0.07 | 3,078 | 37_36_N_138_2_E |
| 6 | A*26:01-B*35:01-C*03:03-DRB1*04:10-DQA1*03:03-DQB1*04:02-DPA1*02:02-DPB1*05:01 | Japan pop 17 | 0.07 | 3,078 | 37_36_N_138_2_E |
| 7 | A*24:02-B*35:01-C*03:03-DRB1*04:10 | Japan pop 16 | 0.06 | 18,604 | 35_41_N_139_46_E |
| 8 | A*31:01-B*35:01-C*03:03-DRB1*04:10 | Japan pop 16 | 0.06 | 18,604 | 35_41_N_139_46_E |
| 9 | A*02:06-B*35:01-C*03:03-DRB1*04:10 | Japan pop 16 | 0.05 | 18,604 | 35_41_N_139_46_E |
| 10 | A*33:03-B*35:01-C*03:03-DRB1*04:10-DQB1*04:02 | USA Asian pop 2 | 0.04 | 1,772 | 44_58_N_93_15_W |
| 11 | A*11:01-B*35:01-C*03:03-DRB1*04:10 | Japan pop 16 | 0.04 | 18,604 | 35_41_N_139_46_E |
| 12 | A*01:01-B*35:01-C*03:03-DRB1*04:10 | Germany DKMS - China minority | 0.04 | 1,282 | 48_31_N_9_3_E |
| 13 | A*02:01-B*35:01-C*03:03-DRB1*04:10-DQA1*03:03-DQB1*04:02-DPA1*01:03-DPB1*02:01 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
| 14 | A*02:01-B*35:01-C*03:03-DRB1*04:10-DQA1*03:03-DQB1*04:02-DPA1*02:02-DPB1*03:01 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
| 15 | A*02:06-B*35:01-C*03:03-DRB1*04:10-DQA1*03:03-DQB1*04:02-DPA1*02:02-DPB1*03:01 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
| 16 | A*24:02-B*35:01-C*03:03-DRB1*04:10-DQA1*03:03-DQB1*04:02-DPA1*01:03-DPB1*02:01 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
| 17 | A*24:02-B*35:01-C*03:03-DRB1*04:10-DQA1*03:03-DQB1*04:02-DPA1*02:02-DPB1*03:01 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
| 18 | A*24:20-B*35:01-C*03:03-DRB1*04:10-DQA1*03:03-DQB1*04:02-DPA1*01:03-DPB1*02:01 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
| 19 | A*26:01-B*35:01-C*03:03-DRB1*04:10-DQA1*03:03-DQB1*04:02-DPA1*01:03-DPB1*04:02 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
| 20 | A*26:02-B*35:01-C*03:03-DRB1*04:10-DQA1*03:03-DQB1*04:02-DPA1*02:02-DPB1*03:01 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
| 21 | A*26:03-B*35:01-C*03:03-DRB1*04:10-DQA1*03:03-DQB1*04:02-DPA1*01:03-DPB1*04:01 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
| 22 | A*31:01-B*35:01-C*03:03-DRB1*04:10-DQA1*03:03-DQB1*04:02-DPA1*01:03-DPB1*04:01 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
| 23 | A*31:01-B*35:01-C*03:03-DRB1*04:10-DQA1*03:03-DQB1*04:02-DPA1*02:02-DPB1*05:01 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
| 24 | A*26:03-B*35:01-C*03:03-DRB1*04:10 | Japan pop 16 | 0.02 | 18,604 | 35_41_N_139_46_E |
| 25 | A*24:20-B*35:01-C*03:03-DRB1*04:10 | Japan pop 16 | 0.02 | 18,604 | 35_41_N_139_46_E |
| 26 | A*26:02-B*35:01-C*03:03-DRB1*04:10 | Japan pop 16 | 0.01 | 18,604 | 35_41_N_139_46_E |
| 27 | A*33:03-B*35:01-C*03:03-DRB1*04:10 | Japan pop 16 | 0.01 | 18,604 | 35_41_N_139_46_E |
| 28 | A*26:01-B*35:01-C*03:03-DRB1*04:10-DQB1*04:02 | Belgium | 0.00 | 31,412 | 51_2_N_4_28_E |
Allele frequency net database (AFND) 2020 update: gold-standard data classification, open access genotype data and new query tools
Gonzalez-Galarza FF, McCabe A, Santos EJ, Jones J, Takeshita LY, Ortega-Rivera ND, Del Cid-Pavon GM, Ramsbottom K, Ghattaoraya GS, Alfirevic A, Middleton D and Jones AR Nucleic Acid Research 2020, 48:D783-8.
Liverpool, U.K.
support@allelefrequencies.net