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: ss3874733295           
Submitter
HandleSGDP_PRJ
Submitter SNP IDSGDP_10_89686083
RefSNP(rs#)clustering in process
Submitted Batch IDSGDP_279_public
Submitted DateNov 04, 2019
Publication CitedN.D.
First entry to dbSNPNov 4 2019 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA
Ascertainment Samplesize558
PopulationSGDP_279_public
Allele
Observed AlleleT/C
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|ss3874733295|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic
 AATTTATCTG TAATTTAGTG ATCTT
 Y
 CTAGTGTGAT AAAACGTCAG AAGTA

  Submitted Frequency for ss3874733295 back to top
There is no frequency submission for ss3874733295.


  dbSNP summary of Genotypes for ss3874733295 back to top
No sufficient data to compute Hardy-weinberg probability for ss3874733295.


  Submitted individual genotype for ss3874733295 back to top
There is no individual genotype data for ss3874733295.