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: ss712336891           
Submitter
HandleNHLBI-ESP
Submitter SNP IDESP6500SI-chr1-154542216
RefSNP(rs#)rs8192485
Submitted Batch IDESP6500SI
Submitted DateFeb 20, 2013
Publication CitedN.D.
First entry to dbSNPFeb 20 2013 12:00:00:000AM
Assay
SpeciesHomo sapiens
Molecular
Type
Genomic
MethodEXOME CAPTURE AND SEQUENCING
Ascertainment Samplesize10300
PopulationESP_Cohort_Populations
Allele
Observed AlleleA/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|ss712336891|allelePos=101|len=201|taxid=9606|alleles='A/G'|mol=Genomic
 ACTGAAATCA GCCCCGCCAA AATGTGTTAA TGCTTGTGTG CTTCCTCCCC TGGTGTTTCC
 AAGGCTTGGG GAGGTGTGAG AGGGACCCTG GGTGGTGGCA
 R
 TGACCCCACA GGCTTAGGGG CCTTCTCGGC AGCCTCTCTT CCTCCCTGCA GCATGAGCGG
 GAGCAGATCA TGACCACCAA TGTCTGGCTG ACCCAGGTAA

  Submitted Frequency for ss712336891 back to top
There is no frequency submission for ss712336891.


  dbSNP summary of Genotypes for ss712336891 back to top
No sufficient data to compute Hardy-weinberg probability for ss712336891.


  Submitted individual genotype for ss712336891 back to top
There is no individual genotype data for ss712336891.