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: ss3995628           
Submitter
HandlePERLEGEN
Submitter SNP IDP00199476
RefSNP(rs#)rs2821571
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 AlleleT/C
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 46660

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss3995628|allelePos=101|len=201|taxid=9606|alleles='T/C'|mol=Genomic
 GTGGGCAATA TCATCAACCC TTGAGGGAAA TTCAAGATAT TCCTAACACA GAAATATTCT
 TAGCTGAAAA GAGTATGGGA TGACAATTTT CAACCTGGCA
 Y
 ATATAAAAAG AAGAAAAATG TTGGGTAAAT GAACAGCAAA AGAAAGATGA CATTCATATG
 TCCTATGCAA TTCTGAATAC TTATTTTATG TAGGTGAATA

  Submitted Frequency for ss3995628 back to top
There is no frequency submission for ss3995628.


  dbSNP summary of Genotypes for ss3995628 back to top
No sufficient data to compute Hardy-weinberg probability for ss3995628.


  Submitted individual genotype for ss3995628 back to top
There is no individual genotype data for ss3995628.