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: ss3759267529           
Submitter
HandleEVA
Submitter SNP IDEVA_PRJNA289433_rs5751738
RefSNP(rs#)clustering in process
Submitted Batch IDPRJNA289433
Submitted DateNov 16, 2018
Publication CitedN.D.
First entry to dbSNPNov 16 2018 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA HISEQ 2500
Ascertainment Samplesize21280
PopulationN.D.
Allele
Observed AlleleG/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|ss3759267529|allelePos=26|len=51|taxid=9606|alleles='G/C'|mol=Genomic
 CTGTGTGTTA CGTGGGAACA GTCCC
 S
 TTTCCTGCCA GCTGCCTGTC AGGCA

  Submitted Frequency for ss3759267529 back to top
There is no frequency submission for ss3759267529.


  dbSNP summary of Genotypes for ss3759267529 back to top
No sufficient data to compute Hardy-weinberg probability for ss3759267529.


  Submitted individual genotype for ss3759267529 back to top
There is no individual genotype data for ss3759267529.