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Submitted SNP(ss) Details: ss3634303484           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmniExpressExome-8v1-2_A_rs9424284-131_B_F_1895000740
RefSNP(rs#)clustering in process
Submitted Batch IDHumanOmniExpressExome-8v1-2_A
Submitted DateDec 07, 2017
Publication CitedN.D.
First entry to dbSNPDec 7 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize964193
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|ss3634303484|allelePos=26|len=51|taxid=9606|alleles='T/C'|mol=Genomic
 AAGGATGTGA GGTGCACACT GGCTT
 Y
 GGGGAGGATG AGTTACACAG GGGGT

  Submitted Frequency for ss3634303484 back to top
There is no frequency submission for ss3634303484.


  dbSNP summary of Genotypes for ss3634303484 back to top
No sufficient data to compute Hardy-weinberg probability for ss3634303484.


  Submitted individual genotype for ss3634303484 back to top
There is no individual genotype data for ss3634303484.