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: ss2632742306           
Submitter
HandleILLUMINA
Submitter SNP IDSoL_HCHS_Custom_15041502_B3_RefStrand_rs11202607-131_T_R_1886407
RefSNP(rs#)rs11202607
Submitted Batch IDSoL_HCHS_Custom_15041502_B3_RefStrand
Submitted DateFeb 02, 2017
Publication CitedN.D.
First entry to dbSNPFeb 2 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize2536661
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
Homozygote Detected
PCR Confirmed
In Expressed Sequence
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss2632742306|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 CAATTTCGGG CACCGCATAT TAAAA
 Y
 GTAACTTTAT TGTTCCAATA TGTAA

  Submitted Frequency for ss2632742306 back to top
There is no frequency submission for ss2632742306.


  dbSNP summary of Genotypes for ss2632742306 back to top
No sufficient data to compute Hardy-weinberg probability for ss2632742306.


  Submitted individual genotype for ss2632742306 back to top
There is no individual genotype data for ss2632742306.