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: ss3726656077           
Submitter
HandleILLUMINA
Submitter SNP IDMulti-EthnicGlobal_D2_rs28358584-138_T_F_2264367344
RefSNP(rs#)clustering in process
Submitted Batch IDMulti-EthnicGlobal_D2
Submitted DateNov 09, 2018
Publication CitedN.D.
First entry to dbSNPNov 9 2018 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize1748250
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|ss3726656077|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic
 CTGACGCCAT AAAACTCTTC ACCAA
 R
 GAGCCCCTAA AACCCGCCAC ATCTA

  Submitted Frequency for ss3726656077 back to top
There is no frequency submission for ss3726656077.


  dbSNP summary of Genotypes for ss3726656077 back to top
No sufficient data to compute Hardy-weinberg probability for ss3726656077.


  Submitted individual genotype for ss3726656077 back to top
There is no individual genotype data for ss3726656077.