SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 241
OMIM_ID 603903
Disease SICKLE CELL ANEMIA
Gene

HBB

SNP_ID

rs10742584

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles A/G
Orientation fwd/T
Chr-Number 11
SNP type R
Length 451
5' Near Seq 30 bp acaggacagaatggatgaaaactctacctc
3' Near Seq 30 bp gttctaagcatatcttctccttatttggat
Fasta Sequence ATATTTGGAA TCACAGCTTG GTAAGCATAT TGAAGATCGT TTTCCCAATT TTCTTATTAC ACAAATAAGA AGTTGATGCA CTAAAAGTGG AAGAGTTTTG TCTACCATAA TTCAGCTTTG GGATATGTAG ATGGATCTCT TCCTGCGTCT CCAGAATATG CAAAATACTT ACAGGACAGA ATGGATGAAA ACTCTACCTC R GTTCTAAGCA TATCTTCTCC TTATTTGGAT TAAAACCTTC TGGTAAGAAA AGAAAAAata tatatatata tgtgtgtata tatacacaca tacatataca tatatatGCA TTCATTTGTT GTTGTTTTTC TTAATTTGCT CATGCATGCT AATAAATTAT GTCTAAAAAT AGAATAAATA CAAATCAATG TGCTCTGTGC ATTAGTTACT TATTAGGTTT TGGGAAACAA GAGATAAAAA ACTAGAGACC
     

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