HLA > Haplotype Frequency Search
Please specify your search by selecting options from boxes. Then, click "Search" to find HLA Haplotype frequencies
that match your criteria. Remember at least one option must be selected.
Displaying 1 to 13
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Line |
Haplotype |
Population |
Frequency (%) |
Sample Size |
Distribution¹ |
1 | A*24:02-B*39:01-DRB1*08:03 | | New Zealand Maori with Full Ancestry | 4.3000 | | 46 |
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2 | A*24:02-B*39:01-DRB1*08:03 | | New Zealand Maori with Admixed History | 3.8095 | | 105 |
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3 | A*24:02-B*39:01-DRB1*08:03 | | Taiwan Tzu Chi Morrow Donor Registry Aborigine | 2.9860 | | 233 |
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4 | A*24:02:01-B*39:01:01-C*07:02:01-DRB1*08:03:02-DQB1*06:01:01 | | China Zhejiang Han | 0.2774 | | 1,734 |
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5 | A*24:02-B*39:01-C*07:02-DRB1*08:03-DQB1*06:01 | | USA NMDP Hawaiian or other Pacific Islander | 0.2329 | | 11,499 |
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6 | A*24:02-B*39:01-DRB1*08:03 | | Hong Kong Chinese cord blood registry | 0.1321 | | 3,892 |
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7 | A*24:02-B*39:01-C*07:02-DRB1*08:03 | | Japan pop 16 | 0.1200 | | 18,604 |
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8 | A*24:02-B*39:01-C*07:02-DRB1*08:03 | | Germany DKMS - China minority | 0.1100 | | 1,282 |
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9 | A*24:02-B*39:01-C*07:02-DRB1*08:03 | | Hong Kong Chinese BMDR | 0.0849 | | 7,595 |
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10 | A*24:02-B*39:01-C*07:02-DRB1*08:03-DQA1*01:03-DQB1*06:01-DPA1*01:03-DPB1*02:01 | | Japan pop 17 | 0.0700 | | 3,078 |
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11 | A*24:02:01-B*39:01:01-C*07:02:01-DRB1*08:03:02-DPB1*05:01:01 | | Hong Kong Chinese HKBMDR HLA 11 loci | 0.0370 | | 5,266 |
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12 | A*24:02-B*39:01-C*12:03-DRB1*08:03-DQB1*03:01 | | Germany DKMS - Turkey minority | 0.0310 | | 4,856 |
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13 | A*24:02:01-B*39:01:01-C*07:02:01-DRB1*08:03:02-DPB1*02:02:01 | | Hong Kong Chinese HKBMDR HLA 11 loci | 0.0215 | | 5,266 |
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Notes:
* Haplotype Frequencies: Total number of copies of the haplotype in the population sample (Haplotypes / 2n) shown in percentages (%).
Important: This field has been expanded to two decimals to better represent frequencies of large datasets (e.g. where sample size > 1000 individuals)
¹ Distribution - Shows the geographic distribution in overlaid maps of the complete haplotype (left icon) or the input alleles if low level resolution was entered (right icon).