Previous studies have reported a high incidence of hemoglobin E (HbE) in Northeast Indian populations. In the present study 10 endogamous populations of Assam belonging to two racial groups, Caucasoid and Mongoloid, were examined. The frequency of HbE gene (Hb βE) in the Caucasoid caste populations is around 0.1, whereas the gene is highly prevalent in the Mongoloid populations, frequencies ranging between 0.2 and 0.6. Predominance of Hb βE in the Tibeto-Burman speakers is contrary to observations made in Southeast Asia, where an association between Austro-Asiatic speakers and high prevalence of HbE exist. The highest occurrence of the gene in this area, which is on the far end of the proposed centre of distribution in Northern Kampuchea and Northeast Thailand, is also a deviation from the expected pattern of gene distribution. It is speculated that Hb βE in the Tibeto-Burman populations of Assam arose by an independent mutation which contributed to the high frequencies of Hb βE in the Northeast Indian populations.

Esterase-D phenotypes have been determined electrophoretically among the two regional groups of the Yanadi tribe of Andhra Pradesh in South India. The identified esterase-D² (EsD²) gene frequencies among the coastal, interior and pooled Yanadis are 0.4320, 0.3562 and 0.3989, respectively.

Transferrin subtypes have been determined by isoelectric focussing of sera from 536 individuals belonging to 9 South Indian populations: Vaidic Brahmins and Vaysya from Andhra Pradesh; Havik Brahmin, Lingayat and Jenu Kuruba from Karnataka; Namboodri Brahmin, Ezhava and Urali from Kerala; and Kalian from Tamil Nadu. C1 and C2 alleles are present in all the populations, whereas C4 is totally lacking and D1 occurs only in 3 populations. The highest frequency of Cl gene (0.814) is found in Havik Brahmins while C2 shows highest incidence among the tribe Urali. C1 occurs in slightly higher frequencies among the Hindu castes (range 0.724–0.814) than the tribal populations (range 0.698–0.703). C2 is more common in the tribes (range 0.281–0.290) compared to the castes (range 0.186–0.269). Strikingly the C3 allele is absent in all the 3 Brahmin samples but is present in 3 non-Brahmin castes and a tribal population. An examination of all the available data on Tf subtypes in India reveals no clear-cut decreasing north-south gradient in C1 gene as suggested by Walter et al. (1983). Interestingly, however, the same is observed when tribal populations are considered separately. Among the castes, in fact, the opposite trend (increasing north to south) is seen. It is suggested that the basic postulate of Walter et al. (1983) will hold good only among the tribal populations of the country. The data do not fully support the observation of Kamboh and Kirk (1983) that C3 is a specific marker of European (Caucasian) populations.

Red cell hemolysates from 1,004 persons belonging to 14 population groups drawn from four South Indian states, Andhra Pradesh, Tamil Nadu, Karnataka, and Kerala, were tested for PGM1 subtypes. The groups are characterized by a high frequency of phenotype 1+1+ (range 36.98-71.64%) and the allele 1+ (range 60-79%). The groups exhibit marked heterogeneity for PGM1 locus. The results show a clear demarcation between tribes and Brahmin groups.

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