SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 234
OMIM_ID 603903
Disease SICKLE CELL ANEMIA
Gene

HBB

SNP_ID

rs33941377

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles A/C/G/T
Orientation fwd/B
Chr-Number 11
SNP type N
Length 101
5' Near Seq 30 bp tcacttagacctcaccctgtggagccacac
3' Near Seq 30 bp ctagggttggccaatctactcccaggagca
Fasta Sequence AAGGACAGGT ACGGCTGTCA TCACTTAGAC CTCACCCTGT GGAGCCACAC N CTAGGGTTGG CCAATCTACT CCCAGGAGCA GGGAGGGCAG GAGCCAGGGC
     

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