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: ss536686110           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni5-4v1_B_rs11202607-131_T_R_1886407518
RefSNP(rs#)rs11202607
Submitted Batch IDHumanOmni5-4v1_B
Submitted DateJun 22, 2012
Publication CitedN.D.
First entry to dbSNPJun 22 2012 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize2
PopulationN.D.
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 SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss536686110|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 CAATTTCGGG CACCGCATAT TAAAA
 Y
 GTAACTTTAT TGTTCCAATA TGTAA

  Submitted Frequency for ss536686110 back to top
There is no frequency submission for ss536686110.


  dbSNP summary of Genotypes for ss536686110 back to top
No sufficient data to compute Hardy-weinberg probability for ss536686110.


  Submitted individual genotype for ss536686110 back to top
There is no individual genotype data for ss536686110.