SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 237
OMIM_ID 603903
Disease SICKLE CELL ANEMIA
Gene

HBB

SNP_ID

rs34883338

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/T
Orientation fwd/B
Chr-Number 11
SNP type Y
Length 101
5' Near Seq 30 bp tgtcatcacttagacctcaccctgtggagc
3' Near Seq 30 bp acaccctagggttggccaatctactcccag
Fasta Sequence GAGCCAAGGA CAGGTACGGC TGTCATCACT TAGACCTCAC CCTGTGGAGC Y ACACCCTAGG GTTGGCCAAT CTACTCCCAG GAGCAGGGAG GGCAGGAGCC
     

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