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: ss479154477           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni1-Quad_v1-0_C_ABO_SNP1-0_T_R_1859003001
RefSNP(rs#)rs77805226
Submitted Batch IDHumanOmni1-Quad_v1-0_C
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 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|ss479154477|allelePos=26|len=51|taxid=9606|alleles='G/A'|mol=Genomic
 ATGGTGGTGT TCTGGAGCCT GAACT
 R
 CTCGTTGAGG ATGTCGATGT TGAAT

  Submitted Frequency for ss479154477 back to top
There is no frequency submission for ss479154477.


  dbSNP summary of Genotypes for ss479154477 back to top
No sufficient data to compute Hardy-weinberg probability for ss479154477.


  Submitted individual genotype for ss479154477 back to top
There is no individual genotype data for ss479154477.