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: ss3022981659           
Submitter
HandleILLUMINA
Submitter SNP IDMEGA_Consortium_v2_15070954_A2_MitoA11252G-0_B_R_1852011184
RefSNP(rs#)clustering in process
Submitted Batch IDMEGA_Consortium_15070954_A2
Submitted DateJun 28, 2017
Publication CitedN.D.
First entry to dbSNPJun 28 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize2036060
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|ss3022981659|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic
 GCTCCCTTCC CCTACTCATC GCACT
 R
 ATTTACACTC ACAACACCCT AGGCT

  Submitted Frequency for ss3022981659 back to top
There is no frequency submission for ss3022981659.


  dbSNP summary of Genotypes for ss3022981659 back to top
No sufficient data to compute Hardy-weinberg probability for ss3022981659.


  Submitted individual genotype for ss3022981659 back to top
There is no individual genotype data for ss3022981659.