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: ss3643208322           
Submitter
HandleILLUMINA
Submitter SNP IDHuman1Mv1_C_rs16987048-123_B_F_IFB1161149544:0
RefSNP(rs#)clustering in process
Submitted Batch IDHuman1Mv1_C
Submitted DateJan 02, 2018
Publication CitedN.D.
First entry to dbSNPJan 2 2018 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize1072820
PopulationN.D.
Allele
Observed AlleleT/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|ss3643208322|allelePos=26|len=51|taxid=9606|alleles='T/G'|mol=Genomic
 AACCGCTTTT GGCAGACGTC ACACA
 K
 GTAGGGCCTC TCGCCAGTGT GGACT

  Submitted Frequency for ss3643208322 back to top
There is no frequency submission for ss3643208322.


  dbSNP summary of Genotypes for ss3643208322 back to top
No sufficient data to compute Hardy-weinberg probability for ss3643208322.


  Submitted individual genotype for ss3643208322 back to top
There is no individual genotype data for ss3643208322.