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: ss139616103           
Submitter
HandleENSEMBL
Submitter SNP IDENSSNP12578667
RefSNP(rs#)rs1801260
Submitted Batch ID2008-11-watson_3
Submitted DateMay 18, 2009
Publication CitedN.D.
First entry to dbSNPMay 18 2009 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type		Genomic
MethodENSEMBL-SSAHA
Ascertainment Samplesize2
PopulationENSEMBL_Watson
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 Summarypopulation count: 1
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss139616103|allelePos=102|len=203|taxid=9606|alleles='A/G'|mol=Genomic
 TCCCTGGAGG TCATTTCATA GCTGAGCTTC TTAATATTTG GCAATATATT CTTTTTCCAT
 CAAAAAATAT CCAGGCACCT AAAACACTGT CAGAACTGGC T
 R
 TGCCCCTATG ATCACCTCCT GCTGGCTGGT ATTTAATGTA CATCTGTAGC ACTAGGCAGC
 ATTTTCTCTG CCAACTAATT CCAGGAACTA GAACACTCAA T

  Submitted Frequency for ss139616103 back to top
There is no frequency submission for ss139616103.


  dbSNP summary of Genotypes for ss139616103 back to top
No sufficient data to compute Hardy-weinberg probability for ss139616103.


  Submitted individual genotype for ss139616103 back to top
There is no individual genotype data for ss139616103.

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