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Submitted SNP(ss) Details: ss3635265726           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmniExpress-24v1-1_A_rs4018608-138_T_F_2263595124
RefSNP(rs#)clustering in process
Submitted Batch IDHumanOmniExpress-24v1-1_A
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 Samplesize713014
PopulationN.D.
Allele
Observed AlleleT/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|ss3635265726|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic
 ACTCTGGAGA CTCCAAGGCA CTCAC
 Y
 GGGCAGAGCA GCTGTCTTCC TGGTA

  Submitted Frequency for ss3635265726 back to top
There is no frequency submission for ss3635265726.


  dbSNP summary of Genotypes for ss3635265726 back to top
No sufficient data to compute Hardy-weinberg probability for ss3635265726.


  Submitted individual genotype for ss3635265726 back to top
There is no individual genotype data for ss3635265726.