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Submitted SNP(ss) Details: ss3744179719           
Submitter
HandleILLUMINA
Submitter SNP IDHumanCore-12v1-0_B_rs3748932-131_B_R_2087478498
RefSNP(rs#)clustering in process
Submitted Batch IDHumanCore-12-v1-0_B
Submitted DateNov 14, 2018
Publication CitedN.D.
First entry to dbSNPNov 14 2018 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize298930
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|ss3744179719|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 TACGTCACCC AGTGAATGAT GTGGT
 Y
 CCCAAACTGA AGGTCTAGCC ATCTG

  Submitted Frequency for ss3744179719 back to top
There is no frequency submission for ss3744179719.


  dbSNP summary of Genotypes for ss3744179719 back to top
No sufficient data to compute Hardy-weinberg probability for ss3744179719.


  Submitted individual genotype for ss3744179719 back to top
There is no individual genotype data for ss3744179719.