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: ss1077032300           
Submitter
HandleJMKIDD_LAB
Submitter SNP IDHGDP_WGS_chr10_62523776
RefSNP(rs#)rs2448334
Submitted Batch IDHGDP_WGS
Submitted DateJul 10, 2014
Publication CitedN.D.
First entry to dbSNPJul 10 2014 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodHGDP_WGS_SEQ
Ascertainment Samplesize2
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
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss1077032300|allelePos=26|len=51|taxid=9606|alleles='C/G'|mol=Genomic
 GCAGAGGTTG CAGTGAACCA AGATA
 S
 TGCCACTGCA CTCCAGTCTG GGCAA

  Submitted Frequency for ss1077032300 back to top
There is no frequency submission for ss1077032300.


  dbSNP summary of Genotypes for ss1077032300 back to top
No sufficient data to compute Hardy-weinberg probability for ss1077032300.


  Submitted individual genotype for ss1077032300 back to top
There is no individual genotype data for ss1077032300.