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Submitted SNP(ss) Details: ss3631613842           
Submitter
HandleILLUMINA
Submitter SNP IDHumanOmni2.5-8v1_C_rs3748932-131_B_R_1869436470
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 AlleleC/T
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|ss3631613842|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 TACGTCACCC AGTGAATGAT GTGGT
 Y
 CCCAAACTGA AGGTCTAGCC ATCTG

  Submitted Frequency for ss3631613842 back to top
There is no frequency submission for ss3631613842.


  dbSNP summary of Genotypes for ss3631613842 back to top
No sufficient data to compute Hardy-weinberg probability for ss3631613842.


  Submitted individual genotype for ss3631613842 back to top
There is no individual genotype data for ss3631613842.