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Submitted SNP(ss) Details: ss4962141569           
Submitter
HandleTOPMED
Submitter SNP IDTOPMed_freeze_8?chr13_112,753,922
RefSNP(rs#)clustering in process
Submitted Batch IDFreeze 8 variant calls-chr13
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|ss4962141569|allelePos=26|len=51|taxid=9606|alleles='G/C'|mol=Genomic
 GGAATTAAAG AAAGAAGCCA TCTAT
 S
 TTCTTCCTGG GGCATCATTT GAGCT

  Submitted Frequency for ss4962141569 back to top
There is no frequency submission for ss4962141569.


  dbSNP summary of Genotypes for ss4962141569 back to top
No sufficient data to compute Hardy-weinberg probability for ss4962141569.


  Submitted individual genotype for ss4962141569 back to top
There is no individual genotype data for ss4962141569.

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