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Submitted SNP(ss) Details: ss4970118818           
Submitter
HandleTOPMED
Submitter SNP IDTOPMed_freeze_8?chr14_49,620,332
RefSNP(rs#)clustering in process
Submitted Batch IDFreeze 8 variant calls-chr14
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 AlleleC/T
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|ss4970118818|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 ACTTTTCCCC TCCGAAGCAC AGTCA
 Y
 CCGTCAGCAG CCTCGAGGGC TGACG

  Submitted Frequency for ss4970118818 back to top
There is no frequency submission for ss4970118818.


  dbSNP summary of Genotypes for ss4970118818 back to top
No sufficient data to compute Hardy-weinberg probability for ss4970118818.


  Submitted individual genotype for ss4970118818 back to top
There is no individual genotype data for ss4970118818.

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