SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 249
OMIM_ID 603903
Disease SICKLE CELL ANEMIA
Gene

HBB

SNP_ID

rs2187610

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 catcaaactaaaaaatttccacacaaaaaa
3' Near Seq 30 bp aaaacaatgaacaaatgaaaggtgaaccat
Fasta Sequence GGaaaaataa agaagtgagg ctacatcaaa ctaaaaaatt tccacacaaa aaa S aaaacaatga acaaatgaaa ggtgaaccat gaaatggcat atttgcaaac caaatatttc ttaaatattt tggttaatat ccaaaatata taagaaacac agatgattca ataacaaaca aaaaattaaA AATAGGAAAA TAAAAAAatt aaaaagaaga aaatcctgcc atttatgcga gaattgatga acctggagga tgtaaaacta agaaaaataa gcctgacaca aaaagacaaa tactacacaa ccttgctcat atgtgaaaca taaaaaagtc actctcatgg aaacagacag tagaggtatg gtttccaggg gttgggggtg ggagaatcag gaaactatta ctcaaagggt ataaaatttc agttatgtgg gatgaataaa ttctagatat ctaatgtaca gcatcgtgac tgtagttaat tgtactgtaa gtatatttaa aatttg
     

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