To aid studies of the SNPs of human genetic disorders and to assist to find the variations in the disease causing genes, we have constructed a SNP Browser for Human [Homo sapiens] Genetic Disorders. SNPs are the most common form of DNA sequence variation. They are useful polymorphic markers to investigate genes susceptible to diseases or those related to drug responsiveness. Furthermore, a small subset of SNPs directly influences to the quality and/or quantity of the gene product, and increase a risk to certain diseases and to severe side effect by drugs. Through a discovery of a large number of SNPs, we would like to contribute to identification of disease-related genes and there SNPs in the present database. The database is derived from GenBank releases 161, and it contains 494 SNPs of 30 types of human genetic disorders, along with extensive description of each genetic disorder, the disease causing gene and there SNPs. The database contains comprehensive information related to these genetic disorders such as disease description, their symptoms, diagnosis, treatment and related gene description; and SNPs description like SNP name, OMIMID, refseqID, Orientation and strand, allele and its position, Type of SNP, chromosome number and gene sequence. The contents of this database may be browsed from the web (http://www.quickmt.com/projects/snpb/index.htm). Additionally we are planning to include the SNPs information's of rest genetic disorders of human and other diseases.