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: ss3640973131           
Submitter
HandleILLUMINA
Submitter SNP IDHumanCytoSNP-12v2-1_L_rs12124819-131_B_R_1857380364
RefSNP(rs#)clustering in process
Submitted Batch IDHumanCytoSNP-12v2-1_L
Submitted DateDec 29, 2017
Publication CitedN.D.
First entry to dbSNPDec 29 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize294602
PopulationN.D.
Allele
Observed AlleleA/G
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|ss3640973131|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic
 TCATGGGATG GTGTCAGTTT CAGTA
 R
 AAACGATGTC TCTTATTTTG GTCCA

  Submitted Frequency for ss3640973131 back to top
There is no frequency submission for ss3640973131.


  dbSNP summary of Genotypes for ss3640973131 back to top
No sufficient data to compute Hardy-weinberg probability for ss3640973131.


  Submitted individual genotype for ss3640973131 back to top
There is no individual genotype data for ss3640973131.