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: ss3984774936           
Submitter
HandleEVA
Submitter SNP IDrs9424284
RefSNP(rs#)clustering in process
Submitted Batch IDPRJEB36033
Submitted DateJun 26, 2020
Publication CitedN.D.
First entry to dbSNPJun 26 2020 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodWHOLE-GENOME-SEQUENCING
Ascertainment Samplesize140
PopulationPRJEB36033
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|ss3984774936|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic
 AAGGATGTGA GGTGCACACT GGCTT
 Y
 GGGGAGGATG AGTTACACAG GGGGT

  Submitted Frequency for ss3984774936 back to top
There is no frequency submission for ss3984774936.


  dbSNP summary of Genotypes for ss3984774936 back to top
No sufficient data to compute Hardy-weinberg probability for ss3984774936.


  Submitted individual genotype for ss3984774936 back to top
There is no individual genotype data for ss3984774936.