Twenty individuals sampled from Niemcza (dated 776–1000 CE) provide a snapshot of the community’s genetic landscape that complements archaeological findings. Maternal lineages are dominated by haplogroup H (6 individuals), with T (3), J (2), V (2) and the subclade T2b (2). These maternal haplogroups are widespread across prehistoric and historic Central Europe and are commonly interpreted as signatures of long-term local maternal continuity rather than recent wholesale population replacement.
On the paternal side, the dataset records single occurrences of Y-chromosome markers labeled CTS and FGC. Because both appear only once among the male-derived samples, these Y-lineage counts are low and must be interpreted cautiously: singletons cannot robustly characterize paternal structure. The asymmetry between richer mtDNA representation and sparse Y diversity could reflect sampling bias, differential preservation, or genuinely smaller paternal sample sizes in cemeteries sampled.
Overall, the combined genetic picture aligns with an interpretation of Niemcza as a community with broadly Central European maternal ancestry and heterogeneous, poorly resolved paternal inputs. Archaeogenetic comparisons to Iron Age and later medieval datasets could clarify continuity and admixture patterns, but with only 20 samples — and very few Y-chromosome observations — many conclusions remain provisional.