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HLA » Allele Frequency Search
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| Line | Allele | Population | % of individuals that have the allele |
Allele Frequency |
Sample Size |
Location |
|---|---|---|---|---|---|---|
| 1 | DQA1*01:01 | Kiribati | 0.1530 | 62 | 1_28_S_173_2_E | |
| 2 | DQA1*01:02 | Kiribati | 0.1290 | 62 | 1_28_S_173_2_E | |
| 3 | DQA1*01:03 | Kiribati | 0.1130 | 62 | 1_28_S_173_2_E | |
| 4 | DQA1*02:01 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 5 | DQA1*03:01 | Kiribati | 0.2020 | 62 | 1_28_S_173_2_E | |
| 6 | DQA1*04:01 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 7 | DQA1*05:01 | Kiribati | 0.0240 | 62 | 1_28_S_173_2_E | |
| 8 | DQA1*06:01 | Kiribati | 0.3790 | 62 | 1_28_S_173_2_E | |
| 9 | DQB1*02:01 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 10 | DQB1*03:01 | Kiribati | 0.3950 | 62 | 1_28_S_173_2_E | |
| 11 | DQB1*03:02 | Kiribati | 0.2020 | 62 | 1_28_S_173_2_E | |
| 12 | DQB1*03:03 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 13 | DQB1*04:01 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 14 | DQB1*04:02 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 15 | DQB1*05:01 | Kiribati | 0.0160 | 62 | 1_28_S_173_2_E | |
| 16 | DQB1*05:02 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 17 | DQB1*05:03 | Kiribati | 0.1450 | 62 | 1_28_S_173_2_E | |
| 18 | DQB1*06:01 | Kiribati | 0.2260 | 62 | 1_28_S_173_2_E | |
| 19 | DQB1*06:02 | Kiribati | 0.0160 | 62 | 1_28_S_173_2_E | |
| 20 | DQB1*06:03 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 21 | DQB1*06:04 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 22 | DQB1*06:05 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 23 | DRB1*01:01 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 24 | DRB1*01:03 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 25 | DRB1*03:01 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 26 | DRB1*03:02 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 27 | DRB1*04:01 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 28 | DRB1*04:02 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 29 | DRB1*04:03 | Kiribati | 0.2020 | 62 | 1_28_S_173_2_E | |
| 30 | DRB1*04:04 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 31 | DRB1*04:05 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 32 | DRB1*04:06 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 33 | DRB1*04:10 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 34 | DRB1*07 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 35 | DRB1*08:01 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 36 | DRB1*08:02 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 37 | DRB1*08:03 | Kiribati | 0.1130 | 62 | 1_28_S_173_2_E | |
| 38 | DRB1*09:01:02 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 39 | DRB1*10:01 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 40 | DRB1*11:01 | Kiribati | 0.0160 | 62 | 1_28_S_173_2_E | |
| 41 | DRB1*11:02 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 42 | DRB1*12:01 | Kiribati | 0.0080 | 62 | 1_28_S_173_2_E | |
| 43 | DRB1*12:02 | Kiribati | 0.3790 | 62 | 1_28_S_173_2_E | |
| 44 | DRB1*13:01 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 45 | DRB1*13:02 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 46 | DRB1*14:01 | Kiribati | 0.0160 | 62 | 1_28_S_173_2_E | |
| 47 | DRB1*14:04 | Kiribati | 0.0000 | 62 | 1_28_S_173_2_E | |
| 48 | DRB1*14:05 | Kiribati | 0.0160 | 62 | 1_28_S_173_2_E | |
| 49 | DRB1*14:08 | Kiribati | 0.1050 | 62 | 1_28_S_173_2_E | |
| 50 | DRB1*15:01 | Kiribati | 0.0320 | 62 | 1_28_S_173_2_E | |
| 51 | DRB1*15:02 | Kiribati | 0.1130 | 62 | 1_28_S_173_2_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