SNP Browser for Human [Homo spaiens] Genetic Disorders

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ID 252
OMIM_ID 603903
Disease SICKLE CELL ANEMIA
Gene

HBB

SNP_ID

rs11036351

Organism human (Homo sapiens)
Variation Class SNP: single nucleotide polymorphism
Alleles C/T
Orientation fwd/B
Chr-Number 11
SNP type Y
Length 401
5' Near Seq 30 bp atgggacttccatttggggtgggcctatga
3' Near Seq 30 bp agggtaataagacagtagtgaatatcaagc
Fasta Sequence ATCTAGCATC TACCTACCTA GGTATTGAAT AAGAAAAATG AAGTTAAGGT GGTTGATGGT AACACTATGC TAATAACTGC AGAGCCAGAA GCACCATAAG GGACATGATA AGGGAGCCAG CAGACCTCTG ATCTCTTCCT GAATGCTAAT CTTAAACATC CTGAGGAAGA ATGGGACTTC CATTTGGGGT GGGCCTATGA Y AGGGTAATAA GACAGTAGTG AATATCAAGC TACAAAAAGC CGCCTTTCAA ATTCTTCTCA GTCCTAACTT TTCATACTAA GCCCAGTCCT TCCAAAGCAG ACTGTGAAAG AGTGATAGTT CCGGGAGACT AGCACTGCAG ATTCCGGGTC ACTGTGAGTG GGGGAGGCAG GGAAGAAGGG CTCACAGGAC AGTCAAACCA
     

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