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: 

C*18:02
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
	South African Mixed ancestry	10.0	0.0500		50	See
	South African Black	4.9	0.0247		142	See
	Morocco Atlantic Coast Chaouya		0.0070		98	See
	Morocco Settat Chaouya	1.4	0.0070		98	See
	Spain Sevilla	0.4	0.0018		278	See
	Russia Nizhny Novgorod, Russians	0.1	0.0007		1510	See
	Poland BMR	0.1	0.0003		23595	See
	Czech Republic NMDR		0.0001		5099	See
	Netherlands Leiden		0.0000		1305	See
	South Africa Caucasians		0.0000		102	See
	Ireland Northern	0.0	0.0000		1000	See
	USA San Antonio Caucasian		0.0000		222	See
	USA Alaska Yupik		0.0000		252	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
	Cameroon Sawa		0.0000		13	See
	Cameroon Baka Pygmy		0.0000		10	See
	Central African Republic Mbenzele Pygmy	0.0	0.0000		36	See
	China Tibet Region Tibetan		0.0000		158	See
	Italy pop 5		0.0000		975	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.