HLA Database » Allele Report

The list below shows all populations in AFND that contains the allele. If an allele has an entry with a lower resolution this will be shown at the end.

Allele: 

B*27:15
Allele reported 23 time(s) and present in 8 population(s).

Population		Phenotype Frequency (%)	Allele Frequency (in_decimals)		Sample Size	IMGT/HLA¹ Database	Distribution²	Haplotype³ Association	Notesª
	China Hubei Han	0.1	0.0003		3732	See
	Hong Kong Chinese cord blood registry		0.0003		3892	See
	USA NMDP Chinese		0.0001		99672	See
	Hong Kong Chinese HKBMDR HLA 11 loci	0.0	0.0001		5266	See
	Hong Kong Chinese BMDR		0.0001		7595	See
	USA NMDP Vietnamese		0.0000		43540	See
	USA NMDP Filipino		0.0000		50614	See
	USA NMDP North American Amerindian		0.0000		35791	See
	Netherlands Leiden		0.0000		1305	See
	Bulgaria		0.0000		55	See
	Croatia		0.0000		150	See
	Italy Bergamo	0.0	0.0000		101	See
	USA San Antonio Caucasian		0.0000		222	See
	USA South Texas Hispanic		0.0000		194	See
	USA Alaska Yupik		0.0000		252	See
	Morocco Settat Chaouya	0.0	0.0000		98	See
	Morocco Nador Metalsa pop 2		0.0000		73	See
	USA Caucasian Bethesda	0.0	0.0000		307	See
	USA African American Bethesda	0.0	0.0000		187	See
	South Korea pop 3		0.0000		485	See
	USA Philadelphia Caucasian	0.0	0.0000		141	See
	China North Han		0.0000		105	See
	China Tibet Region Tibetan		0.0000		158	See

Notes:

* Allele Frequency: Total number of copies of the allele in the population sample (Alleles / 2n) in decimal format.
   Important: This field has been expanded to four decimals to better represent frequencies of large datasets (e.g. where sample size > 1000 individuals)
* Phenotype Frequency: Percentage of individuals who have the allele or gene (Individuals / n).
* Allele Frequencies shown in green were calculated from Phenotype Frequencies assuming Hardy-Weinberg proportions.

¹ IMGT/HLA Database - For more details of the allele.
² Distribution - Graphical distribution of the allele.
³ Haplotype Association - Find HLA haplotypes with this allele.
ª Notes - See notes for ambiguous combinations of alleles.