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: ss484486958           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni2.5-4v1_D_rs10845840-131_T_R_1857160780
RefSNP(rs#)rs10845840
Submitted Batch IDHumanOmni2.5-4v1_D
Submitted DateJan 30, 2012
Publication CitedN.D.
First entry to dbSNPJan 30 2012 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize2
PopulationN.D.
Allele
Observed AlleleT/C
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|ss484486958|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic
 TTCTCAGTCT CTTTCCAATT TCCTA
 Y
 GTCTGCCTTG ATTGTCTGCT ATGGT

  Submitted Frequency for ss484486958 back to top
There is no frequency submission for ss484486958.


  dbSNP summary of Genotypes for ss484486958 back to top
No sufficient data to compute Hardy-weinberg probability for ss484486958.


  Submitted individual genotype for ss484486958 back to top
There is no individual genotype data for ss484486958.

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