KIR » Genotype information
This module displays all populations that contain this genotype. The list of populations is sorted by frequency in descending order.
Genotype ID: | 29 |
Group: | Bx |
| 3DL1 | 2DL1 | 2DL3 | 2DS4 | 2DL2 | 2DL5 | 3DS1 | 2DS1 | 2DS2 | 2DS3 | 2DS5 | 2DL4 | 3DL2 | 3DL3 | 2DP1 | 3DP1 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Geographic Region | Population | Frequency (%) | Sample Size | Comments | |
|---|---|---|---|---|---|
| South and Central America |  | Trinidad South Asians KIR | 5.56 | 108 | 2DP1, 3DL3, 3DP1 not tested. |
| Western Asia |  | Turkey KIR pop 3 | 2.10 | 187 | |
| Oceania |  | Indonesia Sulawesi Minahasans KIR | 1.70 | 60 | |
| South and Central America | | Trinidad Africans KIR | 1.61 | 62 | 2DP1, 3DL3, 3DP1 not tested. |
| Oceania | | Indonesia Moluccan Islands KIR | 1.60 | 63 | |
| South Asia |  | Pakistan Karachi KIR | 1.28 | 78 | 2DP1, 3DL3, 3DP1 not tested. |
| Western Asia |  | Iran East Azerbaijan Azeri KIR | 1.20 | 84 | |
| South-East Asia |  | China Tibet Lhasa KIR | 1.00 | 102 | |
| Europe |  | Czech Republic KIR | 0.80 | 125 | |
| Europe |  | Sweden Vasterbotten KIR | 0.66 | 150 | 2DP1, 3DP1 not tested. |
| South-East Asia |  | Singapore Chinese KIR pop 2 | 0.50 | 210 | |
| North America |  | Mexico Mestizo Highlands KIR | 0.40 | 257 | 2DP1, 3DP1 not tested. |
| Western Asia | | Iran Fars Persian KIR | 0.40 | 248 | |
| South-East Asia | | China Shenzhen Han KIR pop 2 | 0.20 | 503 | |
| Sub-Saharan Africa |  | Uganda Kampala KIR | 0.20 | 492 | 2DL4, 3DL2, 3DL3, 3DP1 not tested. |
Nearest Genotypes
The following section shows a list of the closest genotypes that are related to this particular genotype.
These genotypes only differ in one gene which is denoted by an X. The list is sorted by the number of populations in descending order.
| 3DL1 | 2DL1 | 2DL3 | 2DS4 | 2DL2 | 2DL5 | 3DS1 | 2DS1 | 2DS2 | 2DS3 | 2DS5 | 2DL4 | 3DL2 | 3DL3 | 2DP1 | 3DP1 | Genotype ID | Pops | Individuals |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| X | 9 | 121 | 398 | |||||||||||||||
| X | 11 | 69 | 137 | |||||||||||||||
| X | 31 | 23 | 43 | |||||||||||||||
| X | 192 | 11 | 14 | |||||||||||||||
| X | 381 | 7 | 20 | |||||||||||||||
| X | 61 | 3 | 3 | |||||||||||||||
| X | 425 | 2 | 4 | |||||||||||||||
| X | 329 | 1 | 1 |
Geographic distribution
| Frequency (%) |
 | |  |  | |  | |  |  | | |  |  | | |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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.
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