SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 254
OMIM_ID 603903
Disease SICKLE CELL ANEMIA
Gene

HBB

SNP_ID

rs10837631

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles A/T
Orientation fwd/B
Chr-Number 11
SNP type W
Length 601
5' Near Seq 30 bp ggtatctctaagcaagagaactgagtggag
3' Near Seq 30 bp caaggctgagagatgcaggataagcaaatg
Fasta Sequence TCTCAGTCCT AACTTTTCAT ACTAAGCCCA GTCCTTCCAA AGCAGACTGT GAAAGAGTGA TAGTTCCGGG AGACTAGCAC TGCAGATTCC GGGTCACTGT GAGTGGGGGA GGCAGGGAAG AAGGGCTCAC AGGACAGTCA AACCATGACC CCTGTTTTTC CTTCTTCAAG TAGACCTCTA TAAGACAACA GAGACAACTA AGGCTGAGTG GCCAGGCGAG GAGAAACCAT CTCGCCGTAA AACATGGAAG GAACACTTCA GGGGAAAGGT GGTATCTCTA AGCAAGAGAA CTGAGTGGAG W CAAGGCTGAG AGATGCAGGA TAAGCAAATG GGTAGTGAAA AGACATTCAT GAGGACAGCT AAAACAATAA GTAATGTAAA ATACAGCATA GCAAAACTTT AACCTCCAAA TCAAGCCTCT ACTTGAATCC TTTTCTGAGG GATGAATAAG GCATATGCAT CAGGGGCTGT TGCCAATGTG CATTAGCTGT TTGCAGCCTC ACCTTCTTTC ATGGAGTTTA AGATATAGTG TATTTTCCCA AGGTTTGAAC TAGCTCTTCA TTTCTTTATG TTTTAAATGC ACTGACCTCC CACATTCCCT
     

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