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Submitted SNP(ss) Details: ss3636458930           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni1-Quad_v1-0_H_rs4618082-131_T_F_1865705334
RefSNP(rs#)clustering in process
Submitted Batch IDHumanOmni1-Quad_v1-0_H
Submitted DateDec 08, 2017
Publication CitedN.D.
First entry to dbSNPDec 8 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize1134514
PopulationN.D.
Allele
Observed AlleleT/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|ss3636458930|allelePos=26|len=51|taxid=9606|alleles='T/A'|mol=Genomic
 AAGGCCTTAT GAACTGTACA GACAA
 W
 ACAGAAGATT ATTCTTATCC TCATT

  Submitted Frequency for ss3636458930 back to top
There is no frequency submission for ss3636458930.


  dbSNP summary of Genotypes for ss3636458930 back to top
No sufficient data to compute Hardy-weinberg probability for ss3636458930.


  Submitted individual genotype for ss3636458930 back to top
There is no individual genotype data for ss3636458930.