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Submitted SNP(ss) Details: ss5113284038           
Submitter
HandleTOPMED
Submitter SNP IDTOPMed_freeze_8?chrX_10,115
RefSNP(rs#)clustering in process
Submitted Batch IDFreeze 8 variant calls-chrX
Submitted DateNov 20, 2020
Publication CitedN.D.
First entry to dbSNPNov 20 2020 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodFREEZE 8
Ascertainment Samplesize264690
Populationfreeze 8 samples
Allele
Observed AlleleG/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|ss5113284038|allelePos=26|len=51|taxid=9606|alleles='G/C'|mol=Genomic
 AAGCAGACTG CCTGAGCCAG CAGTG
 S
 CAACCCAATG GGGTCCCTTT CCATA

  Submitted Frequency for ss5113284038 back to top
There is no frequency submission for ss5113284038.


  dbSNP summary of Genotypes for ss5113284038 back to top
No sufficient data to compute Hardy-weinberg probability for ss5113284038.


  Submitted individual genotype for ss5113284038 back to top
There is no individual genotype data for ss5113284038.