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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*11:01:01-B*39:01:01-C*07:02:01-DRB1*14:54:01-DQB1*03:01:01 | Vietnam Kinh | 0.99 | 101 | 14_5_N_108_27_E |
| 2 | A*02:01:01-B*39:01:01-C*07:02:01-DRB1*14:54:01-DQB1*05:03:01-DPA1*01:03:01-DPB1*02:02:01 | Brazil Barra Mansa Rio State Caucasian | 0.31 | 405 | 22_32_S_44_10_W |
| 3 | A*68:01-B*39:01-C*07:02-DRB1*14:54-DQB1*05:03 | Italy pop 5 | 0.14 | 975 | 45_28_N_9_11_E |
| 4 | A*11:01-B*39:01-C*07:02-DRB1*14:54 | Hong Kong Chinese BMDR | 0.06 | 7,595 | 22_15_N_114_10_E |
| 5 | A*24:02-B*39:01-C*07:02-DRB1*14:54 | Hong Kong Chinese BMDR | 0.06 | 7,595 | 22_15_N_114_10_E |
| 6 | A*02:06-B*39:01-C*07:02-DRB1*14:54 | Japan pop 16 | 0.04 | 18,604 | 35_41_N_139_46_E |
| 7 | A*02:01-B*39:01-C*07:02-DRB1*14:54-DQB1*05:03 | Spain (Catalunya, Navarra, Extremadura, Aaragón, Cantabria, | 0.03 | 4,335 | 41_22_N_2_11_E |
| 8 | A*03:01-B*39:01-C*07:02-DRB1*14:54-DQB1*05:03 | Spain (Catalunya, Navarra, Extremadura, Aaragón, Cantabria, | 0.03 | 4,335 | 41_22_N_2_11_E |
| 9 | A*02:06-B*39:01-C*07:02-DRB1*14:54-DQA1*01:04-DQB1*05:02-DPA1*01:03-DPB1*06:01 | Japan pop 17 | 0.03 | 3,078 | 37_36_N_138_2_E |
| 10 | A*11:01:01-B*39:01:01-C*07:02:01-DRB1*14:54:01-DQB1*05:02:01 | China Zhejiang Han | 0.03 | 1,734 | 27_2_N_118_1_E |
| 11 | A*26:01-B*39:01-C*07:02-DRB1*14:54 | Japan pop 16 | 0.02 | 18,604 | 35_41_N_139_46_E |
| 12 | A*11:02-B*39:01-C*07:02-DRB1*14:54 | Hong Kong Chinese BMDR | 0.02 | 7,595 | 22_15_N_114_10_E |
| 13 | A*24:02-B*39:01-C*07:02-DRB1*14:54 | Japan pop 16 | 0.02 | 18,604 | 35_41_N_139_46_E |
| 14 | A*11:01-B*39:01-C*07:02-DRB1*14:54 | Japan pop 16 | 0.01 | 18,604 | 35_41_N_139_46_E |
| 15 | A*11:01:01-B*39:01:01-C*07:02:01-DRB1*14:54:01-DPB1*05:01:01 | Hong Kong Chinese HKBMDR HLA 11 loci | 0.01 | 5,266 | 22_25_N_114_17_E |
| 16 | A*02:03:01-B*39:01:01-C*07:02:01-DRB1*14:54:01-DPB1*135:01 | Hong Kong Chinese HKBMDR HLA 11 loci | 0.01 | 5,266 | 22_25_N_114_17_E |
| 17 | A*02:01-B*39:01-C*07:02-DRB1*14:54 | Hong Kong Chinese BMDR | 0.01 | 7,595 | 22_15_N_114_10_E |
| 18 | A*03:01-B*39:01-C*07:02-DRB1*14:54 | Hong Kong Chinese BMDR | 0.01 | 7,595 | 22_15_N_114_10_E |
| 19 | A*26:02-B*39:01-C*07:02-DRB1*14:54 | Japan pop 16 | 0.01 | 18,604 | 35_41_N_139_46_E |
| 20 | A*31:01-B*39:01-C*07:02-DRB1*14:54 | Japan pop 16 | 0.01 | 18,604 | 35_41_N_139_46_E |
| 21 | A*02:01:01-B*39:01:01-C*07:02:01-DRB1*14:54:01-DQB1*05:03:01 | Poland BMR | 0.00 | 23,595 | 52_0_N_19_22_E |
| 22 | A*31:01:02-B*39:01:01-C*07:02:01-DRB1*14:54:01-DQB1*05:03:01 | Poland BMR | 0.00 | 23,595 | 52_0_N_19_22_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