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: ss3182322           
Submitter
HandleHGBASE
Submitter SNP IDSNP000064391
RefSNP(rs#)rs1805407
Submitted Batch ID010706_Genomic
Submitted DateJul 09, 2001
Publication Cited[1] HGBASE: a database of SNPs and other variations in and around human genes
[2] Human genetic bi-allelic sequences (HGBASE), a database of intra-genic polymorphisms
First entry to dbSNPJul 9 2001 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodHGBASE_EXCHANGE
Ascertainment SamplesizeN.D.
PopulationN.D.
Allele
Observed AlleleA/G
Ancestral Allele
Allele OriginN/A
SNP ClassSNV
CpG CodenonCpG
Validation
Validation StatusNot Validated
HWE Goodness of Fitnot applicable
Variation
Frequency SubmissionN.D.
Genotype SummaryN.D.
Genotype SubmissionN.D.
HaplotypeN.D.
Comment
SNP-SPECIFIC INFORMATION: Source - Database Refmolecule - DNA Citation - SubmitterName - Gane K. S. Wong

  Fasta sequence   (Legend) back to top
>gnl|dbSNP|ss3182322|allelePos=26|len=51|taxid=9606|alleles='A/G'|mol=Genomic
 GGGCCTCGTC TCAGAGAGCA AAGCA
 R
 ACCTCCCCCA GCTTGCCCTC TCCCA

  Submitted Frequency for ss3182322 back to top
There is no frequency submission for ss3182322.


  dbSNP summary of Genotypes for ss3182322 back to top
No sufficient data to compute Hardy-weinberg probability for ss3182322.


  Submitted individual genotype for ss3182322 back to top
There is no individual genotype data for ss3182322.