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Submitted SNP(ss) Details: ss3640806187           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmniExpressExome-8v1-2_B_rs2661837-131_B_R_1885746917
RefSNP(rs#)clustering in process
Submitted Batch IDHumanOmniExpressExome-8v1-2_B
Submitted DateDec 28, 2017
Publication CitedN.D.
First entry to dbSNPDec 28 2017 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize964193
PopulationN.D.
Allele
Observed AlleleC/G
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|ss3640806187|allelePos=26|len=51|taxid=9606|alleles='C/G'|mol=Genomic
 AGATACTTTC AGGGGATTTT CATAT
 S
 AATGATTGCA TTTTGCCATT GTTCT

  Submitted Frequency for ss3640806187 back to top
There is no frequency submission for ss3640806187.


  dbSNP summary of Genotypes for ss3640806187 back to top
No sufficient data to compute Hardy-weinberg probability for ss3640806187.


  Submitted individual genotype for ss3640806187 back to top
There is no individual genotype data for ss3640806187.