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Submitted SNP(ss) Details: ss4873645349           
Submitter
HandleTOPMED
Submitter SNP IDTOPMed_freeze_8?chr11_5,047,117
RefSNP(rs#)clustering in process
Submitted Batch IDFreeze 8 variant calls-chr11
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/A
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|ss4873645349|allelePos=26|len=51|taxid=9606|alleles='G/A'|mol=Genomic
 GTCCTGTGGA AACATTCGTA TCAAT
 R
 GTATCTATGG GCTTTTTGTA GTTTC

  Submitted Frequency for ss4873645349 back to top
There is no frequency submission for ss4873645349.


  dbSNP summary of Genotypes for ss4873645349 back to top
No sufficient data to compute Hardy-weinberg probability for ss4873645349.


  Submitted individual genotype for ss4873645349 back to top
There is no individual genotype data for ss4873645349.

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