SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 248
OMIM_ID 603903
Disease SICKLE CELL ANEMIA
Gene

HBB

SNP_ID

rs2156919

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/G
Orientation fwd/T
Chr-Number 11
SNP type S
Length 510
5' Near Seq 30 bp attaaaaagaagaaaatcctgccatttatg
3' Near Seq 30 bp gagaattgatgaacctggaggatgtaaaac
Fasta Sequence GGaaaaataa agaagtgagg ctacatcaaa ctaaaaaatt tccacacaaa aaagaaaaca atgaacaaat gaaaggtgaa ccatgaaatg gcatatttgc aaaccaaata tttcttaaat attttggtta atatccaaaa tatataagaa acacagatga ttcaataaca aacaaaaaat taaAAATAGG AAAATAAAAA Aattaaaaag aagaaaatcc tgccatttat g S gagaattgat gaacctggag gatgtaaaac taagaaaaat aagcctgaca caaaaagaca aatactacac aaccttgctc atatgtgaaa cataaaaaag tcactctcat ggaaacagac agtagaggta tggtttccag gggttggggg tgggagaatc aggaaactat tactcaaagg gtataaaatt tcagttatgt gggatgaata aattctagat atctaatgta cagcatcgtg actgtagtta attgtactgt aagtatattt aaaatttg
     

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