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Submitted SNP(ss) Details: ss4918369981           
Submitter
HandleTOPMED
Submitter SNP IDTOPMed_freeze_8?chr12_52,020,925
RefSNP(rs#)clustering in process
Submitted Batch IDFreeze 8 variant calls-chr12
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 Allele-/C
Ancestral AlleleN.D.
Allele OriginN/A
SNP ClassDIV
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|ss4918369981|allelePos=26|len=51|taxid=9606|alleles='-/C'|mol=Genomic
 CAGCCAGAGT GCAGCAGTGT GCTGA
 N
 CCCCTGGTGG GGAGCCGGGA CCATA

  Submitted Frequency for ss4918369981 back to top
There is no frequency submission for ss4918369981.


  dbSNP summary of Genotypes for ss4918369981 back to top
No sufficient data to compute Hardy-weinberg probability for ss4918369981.


  Submitted individual genotype for ss4918369981 back to top
There is no individual genotype data for ss4918369981.