PGG.SNV

Other names: PGG SNV, PGG_SNV

PGG.SNV is database for understanding the evolutionary and medical implications of human single nucleotide variation (SNV) on a population level. It documents more than 300,000 genomes and 10 billion allele frequencies records for diverse human ethnic groups.

Webpage:
https://www.pggsnv.org

Publications:

Tags:

sequence variant single nucleotide polymorphism mapping population genetics population genomics human genetic variation



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