rs52106734 SNP Detail

Summary

• ID
  rs52106734
• Variation Type
  SNP
• Alleles
  C

• Created in dbSNP Build
  128
• Last Updated in dbSNP Build
  132
• Additional Resources
  JBrowse Genome Browser | Ensembl SNPView | UCSC Browser
  

Genome Location and Flanking Sequence

• Location
  Chr2:152610890 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                      T GGTTCAGGGG GAAACTGCGA GCTGTACTGC AGTCTCTTCG
  ACAGCAGCAC GGGCGTGGCT CTGTGGTGGA TCCTGGATTA GAACTTCACC GCCACCATCC
  C
  AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG AGAGAGAGAG
  AGACTATGCC ACAGACAATT AACATCATCT AGCTCTTGTC T                    
  
  C = C
  

  
  Note: Sequence in lower case indicates low-complexity or repetitive sequence

  ---

SNP Assays
and
SNP Consensus

Strain alleles of submitted assays, and consensus values for this SNP

Assay ID	Submitter SNP ID	Submitter Handle	Population	ss orientation	Variation Type	A/J
ss147974165	ENSMUSSNP195808	ENSEMBL	ENSEMBL_Sanger	f	SNP	C
SNP Consensus Information
SNP					Consensus Type	A/J
rs52106734					SNP	C

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr2:152610890 () rs orientation: forward

Symbol	Name	Function Class
Rr567460	regulatory region 567460	1888 bp distal
Rr567462	regulatory region 567462	729 bp distal
Rr567463	regulatory region 567463	636 bp proximal