NCBI
dbSNP

dbVar ClinVar GaP PubMed Nucleotide Protein
Search small variations in dbSNP or large structural variations in dbVar
transparent GIF
Spacer gif
Have a question about dbSNP? Try searching the SNP FAQ Archive!

Spacer gif
Submitted SNP(ss) Details: ss1946047495           
Submitter
HandleILLUMINA
Submitter SNP IDHumanCoreExome-12v1-0_C_rs3748932-131_B_R_2087478498
RefSNP(rs#)rs3748932
Submitted Batch IDHumanCoreExome12v10_c
Submitted DateOct 29, 2015
Publication CitedN.D.
First entry to dbSNPOct 29 2015 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodILLUMINA-CHIP
Ascertainment Samplesize2
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
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss1946047495|allelePos=26|len=51|taxid=9606|alleles='C/T'|mol=Genomic
 TACGTCACCC AGTGAATGAT GTGGT
 Y
 CCCAAACTGA AGGTCTAGCC ATCTG

  Submitted Frequency for ss1946047495 back to top
There is no frequency submission for ss1946047495.


  dbSNP summary of Genotypes for ss1946047495 back to top
No sufficient data to compute Hardy-weinberg probability for ss1946047495.


  Submitted individual genotype for ss1946047495 back to top
There is no individual genotype data for ss1946047495.