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: ss131629880           
Submitter
HandleENSEMBL
Submitter SNP IDENSSNP159
RefSNP(rs#)rs2423989
Submitted Batch ID2008-11
Submitted DateDec 08, 2008
Publication CitedN.D.
First entry to dbSNPDec 8 2008 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodENSEMBL-SSAHA
Ascertainment Samplesize2
PopulationENSEMBL_Venter
Allele
Observed AlleleC/T
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 Summarypopulation count: 1
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss131629880|allelePos=102|len=203|taxid=9606|alleles='C/T'|mol=Genomic
 CTCTTCACTT CCCAGTAGGG GCGGCCGGGC AGAGGCGCCC CTCACCTCCC GGACGGGGTC
 GCAGCCGGGC AGAGGCGCTC CTCACATCCC AGACGGGGCG G
 Y
 GGGACAAAGG CGCTCCCCAC ATCTCAGACG ATGGGCGGCC GGGCAGAGAC GCTCCTCACT
 TCCTAGATGG GATGGCGGCC GGGAAGAGGT GCTCCTCACT T

  Submitted Frequency for ss131629880 back to top
There is no frequency submission for ss131629880.


  dbSNP summary of Genotypes for ss131629880 back to top
No sufficient data to compute Hardy-weinberg probability for ss131629880.


  Submitted individual genotype for ss131629880 back to top
There is no individual genotype data for ss131629880.

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