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Submitted SNP(ss) Details: ss3632010764           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni2.5-8v1_C_kgp8338809-0_T_F_1812282748
RefSNP(rs#)clustering in process
Submitted Batch IDHumanOmni2.5-8v1_C
Submitted DateNov 28, 2017
Publication CitedN.D.
First entry to dbSNPNov 28 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize2379855
PopulationN.D.
Allele
Observed AlleleG/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|ss3632010764|allelePos=26|len=51|taxid=9606|alleles='G/A'|mol=Genomic
 ACAACCTCGA CTACTACAAG AAGAC
 R
 ACCAACGTGA GCCCGGCCCT GGGGT

  Submitted Frequency for ss3632010764 back to top
There is no frequency submission for ss3632010764.


  dbSNP summary of Genotypes for ss3632010764 back to top
No sufficient data to compute Hardy-weinberg probability for ss3632010764.


  Submitted individual genotype for ss3632010764 back to top
There is no individual genotype data for ss3632010764.

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