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Submitted SNP(ss) Details: ss3642211277           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni1S-8v1_H_kgp10699498-0_B_F_1817018598
RefSNP(rs#)clustering in process
Submitted Batch IDHumanOmni1S-8v1_H
Submitted DateDec 29, 2017
Publication CitedN.D.
First entry to dbSNPDec 29 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize1185976
PopulationN.D.
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|ss3642211277|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 TATTTACATT ATGCCAGATC CAGTA
 Y
 ATGCCATTGT TATCCTCTGT TTTTT

  Submitted Frequency for ss3642211277 back to top
There is no frequency submission for ss3642211277.


  dbSNP summary of Genotypes for ss3642211277 back to top
No sufficient data to compute Hardy-weinberg probability for ss3642211277.


  Submitted individual genotype for ss3642211277 back to top
There is no individual genotype data for ss3642211277.

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