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: ss106322363           
Submitter
HandleBGI
Submitter SNP IDBGI_rs912523
RefSNP(rs#)rs912523
Submitted Batch IDYanhuang1_20080807_b
Submitted DateSep 15, 2008
Publication CitedN.D.
First entry to dbSNPSep 15 2008 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodBGI-SEQUENCING
Ascertainment Samplesize2
PopulationN.D.
Allele
Observed AlleleG/A
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|ss106322363|allelePos=101|len=201|taxid=9606|alleles='G/A'|mol=Genomic
 TAGCCAAAAM TTTCTCTTTC CTTGCTCACG GGCAGCTGGG AGGTCAGTCT GTCACAAGTC
 CCAGGCTGTT CATCTGGCAT GTGCAGACAA AGTTCTAAAT
 R
 CCCCCATCCA GGACTGGCTA GATTATTTGT GGGACCCAGT GCAAAATGAA AATGGCAAGC
 CCCTGTTCAA AAATTAAGAA TTTCAAAATG ATGACAAGAG

  Submitted Frequency for ss106322363 back to top
There is no frequency submission for ss106322363.


  dbSNP summary of Genotypes for ss106322363 back to top
No sufficient data to compute Hardy-weinberg probability for ss106322363.


  Submitted individual genotype for ss106322363 back to top
There is no individual genotype data for ss106322363.

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