SNP Browser for Human [Homo spaiens] Genetic Disorders

  Home
  About us
  About Database
  SNPs ?
  Genetic Disorders ?
  Genetic Disorder List
  Genes List
  SNP Registry
  Acknowledgement
  References
  Our Team
  Contact us


ID 230
OMIM_ID 603903
Disease SICKLE CELL ANEMIA
Gene

HBB

SNP_ID

rs33980857

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles A/C/T
Orientation fwd/B
Chr-Number 11
SNP type H
Length 101
5' Near Seq 30 bp agcagggagggcaggagccagggctgggca
3' Near Seq 30 bp aaaagtcagggcagagccatctattgctta
Fasta Sequence TTGGCCAATC TACTCCCAGG AGCAGGGAGG GCAGGAGCCA GGGCTGGGCA H AAAAGTCAGG GCAGAGCCAT CTATTGCTTA CATTTGCTTC TGACACAACT
     

© 2008, IBI Biosolutions Pvt Ltd. INDIA