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. 2026 Feb 3;17:716. doi: 10.1038/s41467-025-65511-7

Table 1.

Frequencies of the HFE c.845 G > A (C282Y) and c.187 C>G (H63D) variants in the UKB by population group

Group N c.845 G>A (p.Cys282Tyr) c.187 C > G (p.His63Asp)
MAC MAF q2 one in MAC MAF
Genomically British 408,780 63,763 0.0780 0.00608 164 123,466 0.1510
German 2088 254 0.0608 0.00370 270 617 0.1477
French 801 80 0.0499 0.00249 401 285 0.1779
Polish 612 42 0.0343 0.00118 849 182 0.1487
Italian 808 31 0.0192 0.00037 2.7k 230 0.1423
Ashkenazi Jewish 2868 71 0.0124 0.00015 6.5k 724 0.1262
Afro-Caribbean 2171 34 0.0078 0.00006 16k 70 0.0161
Sri Lankan 654 3 0.0023 0.00001 190k 133 0.1017
British Indian 5317 23 0.0022 0.00000 213k 834 0.0784
British Pakistani 1645 4 0.0012 0.00000 676k 239 0.0726
Kenyan 1049 2 0.0010 0.00000 1 M 170 0.0810
East Asian 2244 2 0.0004 0.00000 5 M 134 0.0299
West African 1317 0 0.0000 0.00000 >6 M 15 0.0057

The groups in Table 1 are ordered by decreasing MAF of p.Cys282Tyr. Genomically British were identified by UK Biobank (Data field 22006). Otherwise, data were taken from UKB volunteers either reporting birthplaces in Germany, France, Poland, Italy, Sri Lanka or Kenya, who matched the majority ancestry group from that nation using dbscan (Methods), or those self-declaring their ethnicity as Afro-Caribbean, British Indian, British Pakistani or West African. Ashkenazi Jewish and East Asian frequencies are taken from the UKB allele frequency browser, because this ancestry was not available through self-report in UKB and there were too few individuals born in any single East Asian nation, respectively. In this way, the major groups living in the UK (with >500 volunteers in the UKB) are represented.

MAC minor allele count, MAF minor allele frequency, q2 predicted frequency of p.Cys282Tyr homozygotes, themajor risk genotype; ‘one in’ gives the ratio of people in each population group who carry the major risk genotype, k thousand, M million.