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: ss160664009           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni1-Quad_v1-0_B_rs4147532-128_T_F_1526886202
RefSNP(rs#)rs4147532
Submitted Batch IDHumanOmni1-Quad_v1-0_B
Submitted DateAug 04, 2009
Publication CitedN.D.
First entry to dbSNPAug 4 2009 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CUSTOMERIZED-CHIP
Ascertainment Samplesize270
PopulationN.D.
Allele
Observed AlleleA/G
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassSNV
CpG CodeN.D.
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss160664009|allelePos=61|len=121|taxid=9606|alleles='A/G'|mol=Genomic
 AGAATCTGTA TCTATGAAGT GTTTATTTCC CACATTAAAG ACATTTGCGG TAAAGCGATA
 R
 TTTATTCCAA GCTAATCATG ATTAATTTGT AAAGCCAAAG TTAGAAATGT CTTTCATCAA

  Submitted Frequency for ss160664009 back to top
There is no frequency submission for ss160664009.


  dbSNP summary of Genotypes for ss160664009 back to top
No sufficient data to compute Hardy-weinberg probability for ss160664009.


  Submitted individual genotype for ss160664009 back to top
There is no individual genotype data for ss160664009.

GENERAL: Contact Us | Homepage | Announcements |dbSNP Summary | Genome | FTP SERVER | Build History | Handle Request
DOCUMENTATION: FAQ | Searchable FAQ Archive | Overview | How to Submit | RefSNP Summary Info | Database Schema
SEARCH: Entrez SNP | Blast SNP | Batch Query | By Submitter |New Batches | Method | Population | Publication | Batch | Locus Info | Between Marker
NCBI: PubMed | Entrez | BLAST | OMIM | Taxonomy | Structure

Disclaimer     Privacy statement