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: ss3770778579           
Submitter
HandlePAGE_CC
Submitter SNP IDrs149677938
RefSNP(rs#)clustering in process
Submitted Batch IDPAGE-f3v1.major-groups
Submitted DateJan 09, 2019
Publication Cited[1] The PAGE Study: How Genetic Diversity Improves Our Understanding of the Architecture of Complex Traits
First entry to dbSNPJan 9 2019 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodMEGA ARRAY
Ascertainment Samplesize78702
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
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|ss3770778579|allelePos=26|len=51|taxid=9606|alleles='G/A'|mol=Genomic
 GGCAAGAGGC TGGGCCGCTC CCCCC
 R
 TATCAGCAGC GACTGCTTTT CAGAG

  Submitted Frequency for ss3770778579 back to top
There is no frequency submission for ss3770778579.


  dbSNP summary of Genotypes for ss3770778579 back to top
No sufficient data to compute Hardy-weinberg probability for ss3770778579.


  Submitted individual genotype for ss3770778579 back to top
There is no individual genotype data for ss3770778579.