NCBI
dbSNP

dbVar ClinVar GaP PubMed Nucleotide Protein
Search small variations in dbSNP or large structural variations in dbVar
transparent GIF
Spacer gif
Have a question about dbSNP? Try searching the SNP FAQ Archive!

Spacer gif
Submitted SNP(ss) Report in Submission Format
SNP:  Handle|local_snp_id:   PERLEGEN | P00199485
  NCBI Assay Id(ss#):    ss3995635
  Reference SNP Id(rs#): rs2821577

Batch Detail:
Submitter Handle:           PERLEGEN
Submitter Batch ID:         09-01
Entry Date:                 Sep 26, 2001
Molecular type:             Genomic
No. of Chromosomes sampled: 15
Synonym defined:             
Organism:                   Homo sapiens
Population:                 NCBI|NIHPDR
Submitter Method ID:        WAFER_HYB
Citation:
   1. Blocks of Limited Haplotype Diversity Revealed by High-Resolution
   Scanning of Human Chromosome 21

   View citation details:[1] 
Comment:
   For this submission, we required that the minor allele be detected at
   least twice, i.e., a minimum allele frequency of 10% in our sample of
   20 chromosomes.  We also excluded sites where three or more alleles
   were detected.  For validation, 220 out of 227 randomly selected SNP's
   were confirmed by dideoxy sequencing.