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) Details: ss3995640           
Submitter
HandlePERLEGEN
Submitter SNP IDP00199490
RefSNP(rs#)rs2821581
Submitted Batch ID09-01
Submitted DateSep 26, 2001
Publication Cited11721056
First entry to dbSNPSep 26 2001 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodWAFER_HYB
Ascertainment Samplesize11
PopulationNCBI|NIHPDR
Allele
Observed AlleleC/T
Ancestral Allele
Allele OriginN/A
SNP ClassSNV
CpG CodenonCpG
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.
Comment
position 59184

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss3995640|allelePos=101|len=201|taxid=9606|alleles='C/T'|mol=Genomic
 TAAAAAGCCC ATAGTAAGCA AGATGATTAA CAATTTTTAT ATGAACAAAT GTCTTACAAT
 ATTTTAAACA TCTAGAGAAC ACTGATACCG TCTTCACTTA
 Y
 TGACAATGGC ATATTATCAA TTCACTTTTC CAAAGAGAAA GAAGTTACTT CTTTTGACTT
 AGATCTGACT TCTTAAACTG TCAAATGAAG TAGCTGAGTA

  Submitted Frequency for ss3995640 back to top
There is no frequency submission for ss3995640.


  dbSNP summary of Genotypes for ss3995640 back to top
No sufficient data to compute Hardy-weinberg probability for ss3995640.


  Submitted individual genotype for ss3995640 back to top
There is no individual genotype data for ss3995640.