rs108903997 SNP Detail

Summary

• ID
  rs108903997
• Variation Type
  SNP
• Alleles
  C/G

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

Genome Location and Flanking Sequence

• Location
  Chr1:171805760 (GRCm39)
• SNP Orientation to the Genome
  forward

• SNP Reference Flanking Sequence

                        AGGGCTGGGT TTCCAGGTGT GCACCATCAC ACCAGGACCA
  CATGGGAACT TTTTAGTGTG GCAGGGTTGT TCTGTATCTT GACTGTAAGA GTGGTTTTAT
  S
  TTTATATGCC CCAGTACAGG GGAACGCCAG GGCCAAAAAG GGGGAGTGGG TGGGTAGGGG
  ATTGGGGGGG TGGGTATGGG GGACCTTTGG GATAGCATTG                      
  
  S = C/G
  

  
  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	C57BL/6J	DBA/2J
ss120007653	PARCsnp_1.06094	PARC_SEQ	INBRED	f	SNP	C	G
SNP Consensus Information
SNP					Consensus Type	C57BL/6J	DBA/2J
rs108903997					SNP	C	G

Gene/Marker
Associations
and
Function
Classes

MGI genes/markers associated with the SNP

Location: Chr1:171805760 () rs orientation: forward

Symbol	Name	Function Class
Rr423419	regulatory region 423419	1662 bp proximal