Submitter Handle PJP Submitter SNP ID DIP_523136_chr3_3854025 RefSNP(rs#) rs35573665 Submitted Batch ID NSMB2011_INDEL Submitted Date Jan 21, 2011 Publication Cited [1] Impact of chromatin structure on sequence variability in the human genome First entry to dbSNP Jan 21 2011 12:00:00:000AM Resource Links Submitted Gene Name N.D Submitted Gene ID N.D. Submitted SNP Synonyms N.D Submitted linkout N.D Assay Species Homo sapiens Molecular Type Genomic Method TRACESALIGNMENT Ascertainment Samplesize N.D. Population N.D. Allele Observed Allele C/- Ancestral Allele N.D. Allele Origin N/A SNP Class DIV CpG Code N.D. Validation Validation Status Not Validated HWE Goodness of Fit not applicable Variation Frequency Submission N.D. Genotype Summary N.D. Genotype Submission N.D. Haplotype N.D.   Fasta sequence   (Legend) >gnl|dbSNP|ss295085432|allelePos=52|len=103|taxid=9606|alleles='C/-'|mol=Genomic CTTGAGAGCA TTTGGATTGG GGGCAAGGGC TTTATTACTC CTTCCCCCCC C N ATTTTATAAC CCCACACCAA GTGTCAAGAG CTTTAAGGAC CACAACCAAC C   Submitted Frequency for ss295085432 There is no frequency submission for ss295085432.   dbSNP summary of Genotypes for ss295085432 No sufficient data to compute Hardy-weinberg probability for ss295085432.   Submitted individual genotype for ss295085432 There is no individual genotype data for ss295085432.

GENERAL: Contact Us | Homepage | Announcements |dbSNP Summary | Genome | FTP SERVER | Build History | Handle Request
DOCUMENTATION: FAQ | Searchable FAQ Archive | Overview | How to Submit | RefSNP Summary Info | Database Schema
SEARCH: Entrez SNP | Blast SNP | Batch Query | By Submitter |New Batches | Method | Population | Publication | Batch | Locus Info | Between Marker
NCBI: PubMed | Entrez | BLAST | OMIM | Taxonomy | Structure

Disclaimer     Privacy statement