SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 233
OMIM_ID 603903
Disease SICKLE CELL ANEMIA
Gene

HBB

SNP_ID

rs33994806

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles A/C/G
Orientation fwd/T
Chr-Number 11
SNP type V
Length 101
5' Near Seq 30 bp cacttagacctcaccctgtggagccacacc
3' Near Seq 30 bp tagggttggccaatctactcccaggagcag
Fasta Sequence AGGACAGGTA CGGCTGTCAT CACTTAGACC TCACCCTGTG GAGCCACACC V TAGGGTTGGC CAATCTACTC CCAGGAGCAG GGAGGGCAGG AGCCAGGGCT
     

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